Joumaa, Ahmad et al. published their research in Polymers (Basel, Switzerland) in 2020 |CAS: 2358-84-1

The Article related to octene nixantphos rhodium catalyzed core functionalized amphiphilic nanoreactor hydroformylation, raft polymerization, aqueous biphasic catalysis, hydroformylation, nixantphos, polymerization-induced self-assembly, rhodium, water-confined polymeric nanoreactors and other aspects.Formula: C12H18O5

Joumaa, Ahmad; Gayet, Florence; Garcia-Suarez, Eduardo J.; Himmelstrup, Jonas; Riisager, Anders; Poli, Rinaldo; Manoury, Eric published an article in 2020, the title of the article was Synthesis of nixantphos core-functionalized amphiphilic nanoreactors and application to rhodium-catalyzed aqueous biphasic 1-octene hydroformylation.Formula: C12H18O5 And the article contains the following content:

A latex of amphiphilic star polymer particles, functionalized in the hydrophobic core with nixantphos and containing P(MAA-co-PEOMA) linear chains in the hydrophilic shell (nixantphos-functionalized core-crosslinked micelles, or nixantphos@CCM), has been prepared in a one-pot three-step convergent synthesis using reversible addition-fragmentation chain transfer (RAFT) polymerization in water. The synthesis involves polymerization-induced self-assembly (PISA) in the second step and chain crosslinking with di(ethylene glycol) dimethacrylate (DEGDMA) in the final step. The core consists of a functionalized polystyrene, obtained by incorporation of a new nixantphos-functionalized styrene monomer (nixantphos-styrene), which is limited to 1 mol%. The nixantphos-styrene monomer was synthesized in one step by nucleophilic substitution of the chloride of 4-chloromethylstyrene by deprotonated nixantphos in DMF at 60°C, without interference of either phosphine attack or self-induced styrene polymerization The polymer particles, after loading with the [Rh(acac)(CO)2] precatalyst to yield Rh-nixantphos@CCM, function as catalytic nanoreactors under aqueous biphasic conditions for the hydroformylation of 1-octene to yield n-nonanal selectively, with no significant amounts of the branched product 2-methyl-octanal. The experimental process involved the reaction of Oxybis(ethane-2,1-diyl) bis(2-methylacrylate)(cas: 2358-84-1).Formula: C12H18O5

The Article related to octene nixantphos rhodium catalyzed core functionalized amphiphilic nanoreactor hydroformylation, raft polymerization, aqueous biphasic catalysis, hydroformylation, nixantphos, polymerization-induced self-assembly, rhodium, water-confined polymeric nanoreactors and other aspects.Formula: C12H18O5

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Hewawasam, Piyasena et al. published their patent in 2000 |CAS: 141940-37-6

The Article related to arylquinolinone preparation potassium channel opener, quinolinone aryl preparation erectile dysfunction treatment, stroke treatment quinolinone aryl preparation, brain injury treatment quinolinone aryl preparation, sexual dysfunction quinolinone aryl preparation and other aspects.Related Products of 141940-37-6

On June 15, 2000, Hewawasam, Piyasena; Starrett, John E., Jr. published a patent.Related Products of 141940-37-6 The title of the patent was Preparation of 3-substituted-4-arylquinolin-2-one derivatives as calcium-activated potassium (BK) channel openers. And the patent contained the following:

The title compounds (I) [wherein R and R1 = independently H or Me; R2, R3, and R4 = independently H, halogen, NO2, or CF3; R5 = Br, Cl, or NO2; R6 = H or F; R7 = Me, CRR1OH, CHO, C:NOH, COMe, or (un)substituted aryl; m = 0-1; n = 0-6] were prepared by cyclization and further reaction of 1-[2-(acylamino)phenyl]-1-phenylmethanone derivatives For example, 4-(5-chloro-2-hydroxyphenyl)-3-(2-hydroxyethyl)-6-(trifluoromethyl)-2(1H)-quinoline (II) was synthesized in a 5-step sequence starting with acylation of 1-[2-amino-5-(trifluoromethyl)phenyl]-1′-(5-chloro-2-methoxyphenyl)methanone (preparation given) with 3-carbomethoxypropionyl chloride (82%). Subsequent cyclization (100%), dehydration (78%), demethylation (86%), and reduction of the acid yielded II. II activated the cloned BK channel mSlo expressed in Xenopus oocytes, increasing whole cell outward (K+) BK-mediated currents > 200% at 20 μM. In an in vivo erectile function test on diabetic F-344 rats, II (0.1-1 mg/kg) significantly augmented intracavernous pressure/BP responses elicited by submaximal stimulation of the cavernous nerve. As BK channel openers, I are useful in the treatment of disorders which are responsive to the opening of the potassium channels, such as ischemia, stroke, convulsions, epilepsy, asthma, irritable bowel syndrome, migraine, traumatic brain injury, spinal cord injury, sexual dysfunction, and urinary incontinence. The experimental process involved the reaction of tert-Butyl (4-(trifluoromethyl)phenyl)carbamate(cas: 141940-37-6).Related Products of 141940-37-6

The Article related to arylquinolinone preparation potassium channel opener, quinolinone aryl preparation erectile dysfunction treatment, stroke treatment quinolinone aryl preparation, brain injury treatment quinolinone aryl preparation, sexual dysfunction quinolinone aryl preparation and other aspects.Related Products of 141940-37-6

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Fan, Lian-Feng et al. published their research in Organometallics in 2019 |CAS: 10472-24-9

The Article related to asym allylic alkylation keto ester indanone diene palladium catalyst, phosphoramidite palladium chiral allylation catalyst preparation allyl dienyl ketoester, oxo indanecarboxylate cyclopentanecarboxylate asym allylic alkylation palladium phosphoramidite catalyst and other aspects.SDS of cas: 10472-24-9

On October 28, 2019, Fan, Lian-Feng; Wang, Tian-Ci; Wang, Pu-Sheng; Gong, Liu-Zhu published an article.SDS of cas: 10472-24-9 The title of the article was Palladium-Catalyzed Asymmetric Allylic C-H Alkylation of 1,4-Dienes with Cyclic β-Keto Esters. And the article contained the following:

In the presence of chiral phosphoramidite ligand, a palladium-catalyzed asym. allylic C-H alkylation of 1,4-dienes with cyclic β-keto esters has been established to afford chiral α,α-disubstituted β-keto esters I (3, R1 = H, Me, F, OMe, Cl, OCH2CH:CH2, OCH2CCMe; R2 = Me, Et, iPr, tBu, PhCH2; R = alkyl, cycloalkyl, Ph, carboxy, carboxamide) in good to excellent yields, with high levels of regioselectivity, E/Z selectivity, and enantioselectivity. 1,4-Dienes bearing a wide scope of functional groups, such as ketone, chloride, ester, and amide as well, have been nicely tolerated. In addition, preliminary application of this method enables a concise formal synthesis of (-)-tanikolide. The experimental process involved the reaction of Methyl 2-cyclopentanonecarboxylate(cas: 10472-24-9).SDS of cas: 10472-24-9

The Article related to asym allylic alkylation keto ester indanone diene palladium catalyst, phosphoramidite palladium chiral allylation catalyst preparation allyl dienyl ketoester, oxo indanecarboxylate cyclopentanecarboxylate asym allylic alkylation palladium phosphoramidite catalyst and other aspects.SDS of cas: 10472-24-9

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Pastor-Nieto, Maria A. et al. published their research in Contact Dermatitis in 2021 |CAS: 6197-30-4

The Article related to benzyl salicylate allergen sensitization human frontal fibrosing alopecia, allergic contact dermatitis, benzyl salicylate (cas number 118-58-1), fragrance, frontal fibrosing alopecia, gallates, patch tests, photopatch tests, propolis, scarring alopecia, sunscreen and other aspects.Name: 2-Ethylhexyl 2-cyano-3,3-diphenylacrylate

Pastor-Nieto, Maria A.; Gatica-Ortega, Maria E.; Sanchez-Herreros, Consuelo; Vergara-Sanchez, Aranzazu; Martinez-Mariscal, Jaime; De Eusebio-Murillo, Esther published an article in 2021, the title of the article was Sensitization to benzyl salicylate and other allergens in patients with frontal fibrosing alopecia.Name: 2-Ethylhexyl 2-cyano-3,3-diphenylacrylate And the article contains the following content:

Contact sensitization is frequent among patients with frontal fibrosing alopecia (FFA) (52%-76%). To evaluate the frequency of sensitization/photosensitization in an FFA population. A population of FFA patients were patch tested (Spanish Contact Dermatitis Research Group [GEIDAC] baseline; cosmetic and fragrance series), and photopatch tested (sunscreen series). Thirty-six patients (mean age: 64.6 years; 35/36: women) were studied. A history of dermatitis was recorded in 69.4% (frequently involving the face). Overall, 80.5% patients showed pos. patch-test reactions. The most frequently pos. allergens were nickel sulfate (25%), benzyl salicylate (22%), gallates (16.6%), propolis (16.6%), and limonene hydroperoxides (13.8%). Benzyl salicylate was likely relevant to the dermatitis (labeled on personal care products and most patients reporting clin. improvement with allergen avoidance). Patch tests with sunscreens showed pos. reactions to 11 materials (five patients). Photopatch tests were pos. in one case. We speculate a possible relationship between sensitization to benzyl salicylate and FFA. Hypothetically, the most likely explanation is that sensitization to benzyl salicylate involving FFA patients is a consequence of increased exposure to it. It is unclear whether allergen avoidance may impact the prognosis of alopecia. However, it seems to significantly improve the patients quality of life by lessening dermatitis and pruritus. The experimental process involved the reaction of 2-Ethylhexyl 2-cyano-3,3-diphenylacrylate(cas: 6197-30-4).Name: 2-Ethylhexyl 2-cyano-3,3-diphenylacrylate

The Article related to benzyl salicylate allergen sensitization human frontal fibrosing alopecia, allergic contact dermatitis, benzyl salicylate (cas number 118-58-1), fragrance, frontal fibrosing alopecia, gallates, patch tests, photopatch tests, propolis, scarring alopecia, sunscreen and other aspects.Name: 2-Ethylhexyl 2-cyano-3,3-diphenylacrylate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Pettersson, Pontus et al. published their research in Biochimica et Biophysica Acta, Biomembranes in 2021 |CAS: 79642-50-5

The Article related to arabidopsis soluble tata structure oligomer cell membrane, chemical crosslinking, circular dichroism, electron microscopy, fluorescence correlation spectroscopy, light scattering, membrane insertion, membrane leakage, oligomer, twin-arginine translocase, vesicles and other aspects.Related Products of 79642-50-5

On February 1, 2021, Pettersson, Pontus; Patrick, Joan; Jakob, Mario; Jacobs, Malte; Kloesgen, Ralf Bernd; Wennmalm, Stefan; Maeler, Lena published an article.Related Products of 79642-50-5 The title of the article was Soluble TatA forms oligomers that interact with membranes: Structure and insertion studies of a versatile protein transporter. And the article contained the following:

The twin-arginine translocase (Tat) mediates the transport of already-folded proteins across membranes in bacteria, plants and archaea. TatA is a small, dynamic subunit of the Tat-system that is believed to be the active component during target protein translocation. TatA is foremost characterized as a bitopic membrane protein, but has also been found to partition into a soluble, oligomeric structure of yet unknown function. To elucidate the interplay between the membrane-bound and soluble forms we have investigated the oligomers formed by Arabidopsis thaliana TatA. We used several biophys. techniques to study the oligomeric structure in solution, the conversion that takes place upon interaction with membrane models of different compositions, and the effect on bilayer integrity upon insertion. Our results demonstrate that in solution TatA oligomerizes into large objects with a high degree of ordered structure. Upon interaction with lipids, conformational changes take place and TatA disintegrates into lower order oligomers. The insertion of TatA into lipid bilayers causes a temporary leakage of small mols. across the bilayer. The disruptive effect on the membrane is dependent on the liposome’s neg. surface charge d., with more leakage observed for purely zwitterionic bilayers. Overall, our findings indicate that A. thaliana TatA forms oligomers in solution that insert into bilayers, a process that involves reorganization of the protein oligomer. The experimental process involved the reaction of Bis(2,5-dioxopyrrolidin-1-yl) glutarate(cas: 79642-50-5).Related Products of 79642-50-5

The Article related to arabidopsis soluble tata structure oligomer cell membrane, chemical crosslinking, circular dichroism, electron microscopy, fluorescence correlation spectroscopy, light scattering, membrane insertion, membrane leakage, oligomer, twin-arginine translocase, vesicles and other aspects.Related Products of 79642-50-5

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Yamashita, Hiroko et al. published their research in Tetrahedron in 2015 |CAS: 227940-70-7

The Article related to peptide amino bispidine synthesis conformation nmr ir, amino acid disubstituted amino bispidine synthesis, piperidone cyclocondensation benzylamine paraformaldehyde hydantoin bucherer berg cyclization, hydrolysis protection peptide coupling conformation mol modeling and other aspects.Application In Synthesis of tert-Butyl 7-benzyl-9-oxo-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate

On April 15, 2015, Yamashita, Hiroko; Demizu, Yosuke; Misawa, Takashi; Shoda, Takuji; Kurihara, Masaaki published an article.Application In Synthesis of tert-Butyl 7-benzyl-9-oxo-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate The title of the article was Synthesis of a bis-cationic α,α-disubstituted amino acid (9-amino-bispidine-9-carboxylic acid) and its effects on the conformational properties of peptides. And the article contained the following:

A new bis-cationic cyclic amino acid, 9-amino-3,7-diazabicyclo[3.3.1]nonane-9-carboxylic acid (9-amino-bispidine-9-carboxylic acid = Abp), which is available for both solution phase and solid phase peptide synthesis, was designed and synthesized. Furthermore, a heterotripeptide Cbz-Leu-Abp-Ala-OMe containing Abp was prepared, and its dominant conformation was analyzed by examining its NMR and IR spectra and performing mol. modeling. The tripeptide Cbz-Leu-Abp-Ala-OMe formed a β-turn structure as its preferred conformation in solution The experimental process involved the reaction of tert-Butyl 7-benzyl-9-oxo-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate(cas: 227940-70-7).Application In Synthesis of tert-Butyl 7-benzyl-9-oxo-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate

The Article related to peptide amino bispidine synthesis conformation nmr ir, amino acid disubstituted amino bispidine synthesis, piperidone cyclocondensation benzylamine paraformaldehyde hydantoin bucherer berg cyclization, hydrolysis protection peptide coupling conformation mol modeling and other aspects.Application In Synthesis of tert-Butyl 7-benzyl-9-oxo-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Xie, Tao et al. published their research in Angewandte Chemie, International Edition in 2020 |CAS: 2873-29-2

The Article related to polycyclic xanthone fd594 trisaccharide preparation cross coupling cyclization, crystal structure framework stereoselective glycosylation hydroxylation hydrophenanthrenediol xanthone, glycosylation, natural products, oxidative cyclization, total synthesis, xanthones and other aspects.Synthetic Route of 2873-29-2

On March 16, 2020, Xie, Tao; Zheng, Chaoying; Chen, Kuanwei; He, Haibing; Gao, Shuanhu published an article.Synthetic Route of 2873-29-2 The title of the article was Asymmetric Total Synthesis of the Complex Polycyclic Xanthone FD-594. And the article contained the following:

A highly convergent approach was developed to achieve the first asym. and scalable total synthesis of FD-594, a complex polycyclic xanthone natural product from Streptomyces sp. TA-0256, in a longest linear sequence (LLS) of 20 steps. The trans-9,10-dihydrophenanthrene-9,10-diol fragment (B-C-D ring) was generated through a new strategy involving asym. dihydroxylation followed by Cu-mediated oxidative cyclization. Late-stage stereoselective glycosylation assembled the angular hexacyclic framework with a β-linked 2,6-dideoxy trisaccharide fragment. The experimental process involved the reaction of (2R,3S,4R)-2-(Acetoxymethyl)-3,4-dihydro-2H-pyran-3,4-diyl diacetate(cas: 2873-29-2).Synthetic Route of 2873-29-2

The Article related to polycyclic xanthone fd594 trisaccharide preparation cross coupling cyclization, crystal structure framework stereoselective glycosylation hydroxylation hydrophenanthrenediol xanthone, glycosylation, natural products, oxidative cyclization, total synthesis, xanthones and other aspects.Synthetic Route of 2873-29-2

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Kaberova, Zhansaya et al. published their research in Polymers (Basel, Switzerland) in 2020 |CAS: 2358-84-1

The Article related to acrylic hydrogel preparation swelling crosslinking, pgma, phema, artifacts, hydrogel, laser scanning confocal microscopy, morphology, poly(2-hydroxyethyl methacrylate), poly(glycerol monomethacrylate), variable-pressure and environmental scanning electron microscopy and other aspects.HPLC of Formula: 2358-84-1

Kaberova, Zhansaya; Karpushkin, Evgeny; Nevoralova, Martina; Vetrik, Miroslav; Slouf, Miroslav; Duskova-Smrckova, Miroslava published an article in 2020, the title of the article was Microscopic structure of swollen hydrogels by scanning electron and light microscopies: artifacts and reality.HPLC of Formula: 2358-84-1 And the article contains the following content:

The exact knowledge of hydrogel microstructure, mainly its pore topol., is a key issue in hydrogel engineering. For visualization of the swollen hydrogels, the cryogenic or high vacuum scanning electron microscopies (cryo-SEM or HVSEM) are frequently used while the possibility of artifact-biased images is frequently underestimated. The major cause of artifacts is the formation of ice crystals upon freezing of the hydrated gel. Some porous hydrogels can be visualized with SEM without the danger of artifacts because the growing crystals are accommodated within already existing primary pores of the gel. In some non-porous hydrogels the secondary pores will also not be formed due to rigid network structure of gels that counteracts the crystal nucleation and growth. We have tested the limits of true reproduction of the hydrogel morphol. imposed by the swelling degree and mech. strength of gels by investigating a series of methacrylate hydrogels made by crosslinking polymerization of glycerol monomethacrylate and 2-hydroxyethyl methacrylate including their interpenetrating networks. The hydrogel morphol. was studied using cryo-SEM, HVSEM, environmental SEM (ESEM), laser scanning confocal microscopy (LSCM) and classical wide-field light microscopy (LM). The cryo-SEM and HVSEM yielded artifact-free micrographs for limited range of non-porous hydrogels and for macroporous gels. A true non-porous structure was observed free of artifacts only for hydrogels exhibiting relatively low swelling and high elastic modulus above 0.5 MPa, whereas for highly swollen and/or mech. weak hydrogels the cryo-SEM/HVSEM experiments resulted in secondary porosity. In this contribution we present several cases of severe artifact formation in PHEMA and PGMA hydrogels during their visualization by cryo-SEM and HVSEM. We also put forward empirical correlation between hydrogel morphol. and mech. parameters and the occurrence and intensity of artifacts. The experimental process involved the reaction of Oxybis(ethane-2,1-diyl) bis(2-methylacrylate)(cas: 2358-84-1).HPLC of Formula: 2358-84-1

The Article related to acrylic hydrogel preparation swelling crosslinking, pgma, phema, artifacts, hydrogel, laser scanning confocal microscopy, morphology, poly(2-hydroxyethyl methacrylate), poly(glycerol monomethacrylate), variable-pressure and environmental scanning electron microscopy and other aspects.HPLC of Formula: 2358-84-1

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Sugitani, Hatsuo et al. published their research in Bunseki Kagaku in 1992 |CAS: 1985-51-9

The Article related to reverse phase hplc crosslinking agent determination, photosensitive composition hardener determination hplc, acrylate crosslinking agent determination hplc, methacrylate crosslinking agent determination hplc, liquid chromatog acrylate crosslinking agent determination and other aspects.Electric Literature of 1985-51-9

On January 5, 1992, Sugitani, Hatsuo; Fukasawa, Masato; Katou, Kouichi published an article.Electric Literature of 1985-51-9 The title of the article was Analysis of poly-functional acrylates and methacrylates by reversed-phase liquid chromatography with photodiode-array detector. And the article contained the following:

Identification and quant. determination of crosslinking agents in photosensitive materials were studied by reversed-phase liquid chromatog. using a photodiode-array detector. Thirty-two kinds of polyfunctional acrylates and methacrylates (crosslinking agents) were studied. As a result of this study, 30 kinds of the polyfunctional (meth)acrylates were successfully identified and determined by the gradient elution method using MeCN-H2O as the eluent. This method provided good reproducibilities in the elution volumes (0.20∼3.09%) and peak areas (0.34∼0.32%) in each sample. This method was applied to the anal. of crosslinking agents in com. available solid-type and liquid-type photosensitive materials and proved to be a rapid and very accurate method. The experimental process involved the reaction of 2,2-Dimethylpropane-1,3-diyl bis(2-methylacrylate)(cas: 1985-51-9).Electric Literature of 1985-51-9

The Article related to reverse phase hplc crosslinking agent determination, photosensitive composition hardener determination hplc, acrylate crosslinking agent determination hplc, methacrylate crosslinking agent determination hplc, liquid chromatog acrylate crosslinking agent determination and other aspects.Electric Literature of 1985-51-9

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Shapiro, Gideon et al. published their patent in 2008 |CAS: 227940-70-7

The Article related to tricyclic hydroxamic acid preparation histone deacetylase hdac inhibitor, huntington’s disease treatment tricyclic hydroxamic acid preparation hdac inhibitor, dibenzoxazepine preparation histone deacetylase hdac inhibitor dentatorubralpallidoluysian atrophy treatment and other aspects.Safety of tert-Butyl 7-benzyl-9-oxo-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate

On May 8, 2008, Shapiro, Gideon; Moncuso, John; Pierre, Tessier; Leit, Silvana; Deziel, Robert; David, Smil; Richard, Chesworth; Chantigny, Yves Andre; Patrick, Beaulieu published a patent.Safety of tert-Butyl 7-benzyl-9-oxo-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate The title of the patent was Preparation of tricyclic hydroxamic acids as inhibitors of histone deacetylase. And the patent contained the following:

The title compounds I [Z = N(R1)OR2, H; L = a bond, N(OR2); when L = N(OR2), Z = H; when Z = H, L = N(OR2); R1, R2 = H, alkyl, aryl, etc.; J = a bond, :CH-, alkyl, alkyl(heteroalkyl)alkyl, etc.; Q = diazepine, pyrrolidine, diazabicyclo[3.3.1]nonane, etc.; B = dibenzo[b,f][1,4]oxazepine, benzo[b]pyrido[2,3-e][1,4]diazepine, benzo[f]thieno[2,3-b][1,4]oxazepine, etc.;], useful for the inhibition of histone deacetylase, were prepared E.g., a 3-step synthesis of II, starting from 10,11-dihydrodibenz[b,f][1,4]oxazepin-11-one, was given. All exemplified compounds I have an IC50 of ≤ 10 μM against one of more of HDAC-1 through HDAC-11 (data for representative compounds I were given). Pharmaceutical composition comprising the compound I and methods of treating polyglutamine (polyQ) expansion diseases such as Huntington’s disease, are disclosed. The experimental process involved the reaction of tert-Butyl 7-benzyl-9-oxo-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate(cas: 227940-70-7).Safety of tert-Butyl 7-benzyl-9-oxo-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate

The Article related to tricyclic hydroxamic acid preparation histone deacetylase hdac inhibitor, huntington’s disease treatment tricyclic hydroxamic acid preparation hdac inhibitor, dibenzoxazepine preparation histone deacetylase hdac inhibitor dentatorubralpallidoluysian atrophy treatment and other aspects.Safety of tert-Butyl 7-benzyl-9-oxo-3,7-diazabicyclo[3.3.1]nonane-3-carboxylate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics