Zhang, Wen’s team published research in Tetrahedron: Asymmetry in 15 | CAS: 126613-06-7

Tetrahedron: Asymmetry published new progress about 126613-06-7. 126613-06-7 belongs to esters-buliding-blocks, auxiliary class Chiral Diphenols, name is (R)-[1,1′-Binaphthalene]-2,2′-diyl bis(trifluoromethanesulfonate), and the molecular formula is C8H7ClO3, Recommanded Product: (R)-[1,1′-Binaphthalene]-2,2′-diyl bis(trifluoromethanesulfonate).

Zhang, Wen published the artcileAxially chiral P,S-heterodonor ligands with a binaphthalene framework for palladium-catalyzed asymmetric allylic substitutions: experimental investigation on the reversal of enantioselectivity between different alkyl groups on sulfur atom, Recommanded Product: (R)-[1,1′-Binaphthalene]-2,2′-diyl bis(trifluoromethanesulfonate), the publication is Tetrahedron: Asymmetry (2004), 15(21), 3467-3476, database is CAplus.

The enantioselectivity in the palladium-catalyzed asym. allylic alkylation of 1,3-diphenylpropenyl acetate with di-Me malonate using axially chiral P,S-heterodonor ligands BINAPS with different alkyl groups on sulfur atom has been investigated. Their bidentate coordination patterns to a Pd metal center with both P and S atoms have been unambiguously disclosed by X-ray diffraction. The reaction mechanism and the investigation on the reversal of enantioselectivity between different alkyl groups on sulfur atom have been discussed on the basis of the X-ray crystal structure and NMR spectroscopic data.

Tetrahedron: Asymmetry published new progress about 126613-06-7. 126613-06-7 belongs to esters-buliding-blocks, auxiliary class Chiral Diphenols, name is (R)-[1,1′-Binaphthalene]-2,2′-diyl bis(trifluoromethanesulfonate), and the molecular formula is C8H7ClO3, Recommanded Product: (R)-[1,1′-Binaphthalene]-2,2′-diyl bis(trifluoromethanesulfonate).

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Bergkamp, Jesse J.’s team published research in Journal of Porphyrins and Phthalocyanines in 15 | CAS: 50670-76-3

Journal of Porphyrins and Phthalocyanines published new progress about 50670-76-3. 50670-76-3 belongs to esters-buliding-blocks, auxiliary class Benzene,Phenol,Ester, name is Ethyl 4′-hydroxy-[1,1′-biphenyl]-4-carboxylate, and the molecular formula is C15H14O3, Safety of Ethyl 4′-hydroxy-[1,1′-biphenyl]-4-carboxylate.

Bergkamp, Jesse J. published the artcileSynthesis and characterization of silicon phthalocyanines bearing axial phenoxyl groups for attachment to semiconducting metal oxides, Safety of Ethyl 4′-hydroxy-[1,1′-biphenyl]-4-carboxylate, the publication is Journal of Porphyrins and Phthalocyanines (2011), 15(9-10), 943-950, database is CAplus.

A series of axial phenoxy substituted octabutoxy silicon phthalocyanines bearing Et carboxylic ester and di-Et phosphonate groups have been prepared from the corresponding phenols in pyridine. Axial bis-hydroxy silicon phthalocyanine was prepared using an adaptation of a reported protocol from the octabutoxy free-base phthalocyanine. The phenols bear either carboxylic ester or phosphonate groups, which upon deprotection can serve as anchoring groups for attaching the phthalocyanines to semiconducting metal oxides used in dye sensitized solar cells (DSSCs). All the phthalocyanines of the series absorb in the near infra-red region: 758-776 nm. The first oxidation potential for each phenoxy derivative occurs near 0.55 V vs. SCE as measured by cyclic voltammetry, with all falling within a 10 mV range. This indicates that these dyes will have sufficient energy in the photo-excited state to drive the reduction of protons to hydrogen. Taking into account the absorption and electrochem. potentials, these dyes are promising candidates for use in dual-threshold photo-electrochem. cells.

Journal of Porphyrins and Phthalocyanines published new progress about 50670-76-3. 50670-76-3 belongs to esters-buliding-blocks, auxiliary class Benzene,Phenol,Ester, name is Ethyl 4′-hydroxy-[1,1′-biphenyl]-4-carboxylate, and the molecular formula is C15H14O3, Safety of Ethyl 4′-hydroxy-[1,1′-biphenyl]-4-carboxylate.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Xie, Haopu’s team published research in New Journal of Chemistry in 44 | CAS: 517-23-7

New Journal of Chemistry published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C15H21BO2, Recommanded Product: 3-Acetyldihydrofuran-2(3H)-one.

Xie, Haopu published the artcileThermally healable polyurethane with tailored mechanical performance using dynamic crosslinking motifs, Recommanded Product: 3-Acetyldihydrofuran-2(3H)-one, the publication is New Journal of Chemistry (2020), 44(32), 13584-13590, database is CAplus.

Materials with self-healing abilities have gained tremendous attention in recent years but combing excellent mech. performance and splendid self-healing capacity into a single polymer material is still a great challenge. In this study, a self-healing polyurethane (SHP) material was prepared by constructing a dynamic crosslinked network via quadruple hydrogen bonds formed from 5-(2-hydroxyethyl)-6-methyl-2-aminouracil (UPy). The mech. properties of the materials could be conveniently tuned by adjusting the dynamic crosslinked d. The optimal sample, SHP-75, has excellent mech. performance, showing high tensile strength (27.02 MPa), excellent stretchability (1300%), and prominent toughness (111.37 MJ m-3). Despite such great mech. properties, SHP-75 exhibited superior self-healing abilities and could fully obtain its initial mech. strength after repairing at 80°C for 24 h. A self-healing conductive electrode was further constructed to demonstrate its application prospects in the field of sensing.

New Journal of Chemistry published new progress about 517-23-7. 517-23-7 belongs to esters-buliding-blocks, auxiliary class Tetrahydrofuran,Ketone,Ester, name is 3-Acetyldihydrofuran-2(3H)-one, and the molecular formula is C15H21BO2, Recommanded Product: 3-Acetyldihydrofuran-2(3H)-one.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Lu, Ting’s team published research in LWT–Food Science and Technology in 138 | CAS: 121-79-9

LWT–Food Science and Technology published new progress about 121-79-9. 121-79-9 belongs to esters-buliding-blocks, auxiliary class Natural product, name is Propyl 3,4,5-trihydroxybenzoate, and the molecular formula is C10H12O5, Recommanded Product: Propyl 3,4,5-trihydroxybenzoate.

Lu, Ting published the artcileImproving the oxidative stability of flaxseed oil with composite antioxidants comprising gallic acid alkyl ester with appropriate chain length, Recommanded Product: Propyl 3,4,5-trihydroxybenzoate, the publication is LWT–Food Science and Technology (2021), 110763, database is CAplus.

A gallic acid (GA) alkyl ester exerting the best antioxidant effect in flaxseed oil was identified from ten GA alkyl esters with various chain lengths, which was used in combination with other antioxidants including antioxidant of bamboo leaves, ascorbyl palmitate, butylated hydroxytoluene, phytic acid, phospholipid, rosemary extract, tocopherol, tea polyphenols, and tea polyphenol palmitate (TPP) to improve oxidative stability of flaxseed oil. Rancimat induction period, peroxide value, thiobarbituric acid-reactive substances, and ESR assays indicate that myristyl gallate (GA-C14) was the best GA ester. The flaxseed oil containing GA-C14 and TPP demonstrated the best oxidative stability among all the composite antioxidants. Through optimizing the mixture ratio, the flaxseed oil containing 34.4 mg/kg GA-C14 and 480 mg/kg TPP showed the best oxidative stability. Its shelf life was predicted by an accelerated shelf life testing using the Arrhenius model, which was prolonged 4.83-fold compared to the control sample under 25 °C.

LWT–Food Science and Technology published new progress about 121-79-9. 121-79-9 belongs to esters-buliding-blocks, auxiliary class Natural product, name is Propyl 3,4,5-trihydroxybenzoate, and the molecular formula is C10H12O5, Recommanded Product: Propyl 3,4,5-trihydroxybenzoate.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Li, Hongze’s team published research in Journal of the American Chemical Society in | CAS: 5205-11-8

Journal of the American Chemical Society published new progress about 5205-11-8. 5205-11-8 belongs to esters-buliding-blocks, auxiliary class Alkenyl,Benzene,Ester, name is 3-Methylbut-2-en-1-yl benzoate, and the molecular formula is C12H14O2, Category: esters-buliding-blocks.

Li, Hongze published the artcileDirect Intermolecular Anti-Markovnikov Hydroazidation of Unactivated Olefins, Category: esters-buliding-blocks, the publication is Journal of the American Chemical Society, database is CAplus and MEDLINE.

We herein report a direct intermol. anti-Markovnikov hydroazidation method for unactivated olefins, which is promoted by a catalytic amount of bench-stable benziodoxole at ambient temperature This method facilitates previously difficult, direct addition of hydrazoic acid across a wide variety of unactivated olefins in both complex mols. and unfunctionalized commodity chems. It conveniently fills a synthetic chem. gap of existing olefin hydroazidation procedures, and thereby provides a valuable tool for azido-group labeling in organic synthesis and chem. biol. studies.

Journal of the American Chemical Society published new progress about 5205-11-8. 5205-11-8 belongs to esters-buliding-blocks, auxiliary class Alkenyl,Benzene,Ester, name is 3-Methylbut-2-en-1-yl benzoate, and the molecular formula is C12H14O2, Category: esters-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Shi, Yanqin’s team published research in Journal of Applied Polymer Science in 138 | CAS: 31570-04-4

Journal of Applied Polymer Science published new progress about 31570-04-4. 31570-04-4 belongs to esters-buliding-blocks, auxiliary class Mono-phosphine Ligands, name is Tris(2,4-di-tert-butylphenyl) phosphite, and the molecular formula is C8H9BN2O2, Related Products of esters-buliding-blocks.

Shi, Yanqin published the artcileGreen cinnamaldehyde and thymol modified zinc oxide with double synergistic antibacterial effects in polypropylene, Related Products of esters-buliding-blocks, the publication is Journal of Applied Polymer Science (2021), 138(33), 50911, database is CAplus.

The green cinnamaldehyde (CA) and thymol (THY) sep. or successively modified O-ZnO (O-ZnO-CA, O-ZnO-THY, and O-ZnO-CA-THY) were prepared after (3-aminopropyl) triethoxysilane (KH550) was grafted to the surface of ZnO (O-ZnO) and characterized by FTIR, TGA, and SEM. Polypropylene composites (PP/O-ZnO-CA, PP/O-ZnO-THY, and PP/O-ZnO-CA-THY) were prepared by melting the modified O-ZnO and PP. The antibacterial tests showed that the antibacterial rate of PP/O-ZnO-CA and PP/O-ZnO-THY against S. aureus and E. coli was obviously enhanced. It indicated an excellent synergetic antibacterial effect of O-ZnO and the little CA or THY grafted on the surface of O-ZnO. The antibacterial effect of O-ZnO-CA and O-ZnO-THY was related to the hydrophobic and hydrophilic groups contained in CA and THY. Importantly, CA and THY in O-ZnO-CA-THY exhibited another excellent synergetic antibacterial effect against both S. aureus and E. coli. The antibacterial rate of three PP composites containing 4 phr O-ZnO-CA-THY against S. aureus and E. coli reached 95% and 90%, resp. The mechanism was regarded as that CA and THY grafted onto the same O-ZnO improved the contact probability between antibacterial agents and bacteria. Moreover, O-ZnO-CA, O-ZnO-THY, and O-ZnO-CA-THY had excellent migration resistance in the PP matrix.

Journal of Applied Polymer Science published new progress about 31570-04-4. 31570-04-4 belongs to esters-buliding-blocks, auxiliary class Mono-phosphine Ligands, name is Tris(2,4-di-tert-butylphenyl) phosphite, and the molecular formula is C8H9BN2O2, Related Products of esters-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Yang, Wen-Jun’s team published research in Gaodeng Xuexiao Huaxue Xuebao in 15 | CAS: 3052-61-7

Gaodeng Xuexiao Huaxue Xuebao published new progress about 3052-61-7. 3052-61-7 belongs to esters-buliding-blocks, auxiliary class Amine,Benzene,Amide, name is Benzyl diethylcarbamodithioate, and the molecular formula is C3H8N2S, Safety of Benzyl diethylcarbamodithioate.

Yang, Wen-Jun published the artcileEffects of reaction medium on BDC-initiated acrylamide polymerization, Safety of Benzyl diethylcarbamodithioate, the publication is Gaodeng Xuexiao Huaxue Xuebao (1994), 15(11), 1733-5, database is CAplus.

The effects of reaction medium (alc., dioxane, dioxane/alc.) on the heterogeneous polymerization of acrylamide initiated by BDC (benzyl diethyldithiocarbamate) were studied. Heterogeneous polymerization differed from homogeneous solution polymerization initiated by BDC and did not have the character of living radical polymerization The polarity of reaction medium affected the enolization of acrylamide. The polymer yield and polymer mol. weight had different values using different solvents. The UV spectra showed that iniferter functional groups remained in products.

Gaodeng Xuexiao Huaxue Xuebao published new progress about 3052-61-7. 3052-61-7 belongs to esters-buliding-blocks, auxiliary class Amine,Benzene,Amide, name is Benzyl diethylcarbamodithioate, and the molecular formula is C3H8N2S, Safety of Benzyl diethylcarbamodithioate.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Li, Zengji’s team published research in Gaodeng Xuexiao Huaxue Xuebao in 10 | CAS: 3052-61-7

Gaodeng Xuexiao Huaxue Xuebao published new progress about 3052-61-7. 3052-61-7 belongs to esters-buliding-blocks, auxiliary class Amine,Benzene,Amide, name is Benzyl diethylcarbamodithioate, and the molecular formula is C12H17NS2, HPLC of Formula: 3052-61-7.

Li, Zengji published the artcileStudy on living radical polymerization by using BDC as the photoiniferter, HPLC of Formula: 3052-61-7, the publication is Gaodeng Xuexiao Huaxue Xuebao (1989), 10(1), 83-6, database is CAplus.

Photopolymerization of styrene using benzyl N,N-diethyldithioaminoformate (BDC) as iniferter was studied. Both the yield and average mol. weight of the polymer increased with increasing polymerization time. Polymers with functional end groups were obtained. During the polymerization, the stable small radical which was produced by photolysis of BDC or functional end groups and the propagating radical of styrene were determined by ESR. The living radical polymerization mechanism was explained.

Gaodeng Xuexiao Huaxue Xuebao published new progress about 3052-61-7. 3052-61-7 belongs to esters-buliding-blocks, auxiliary class Amine,Benzene,Amide, name is Benzyl diethylcarbamodithioate, and the molecular formula is C12H17NS2, HPLC of Formula: 3052-61-7.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Zhu, Yun-fei’s team published research in Zhongguo Xinyao Zazhi in 17 | CAS: 924-99-2

Zhongguo Xinyao Zazhi published new progress about 924-99-2. 924-99-2 belongs to esters-buliding-blocks, auxiliary class Alkenyl,Amine,Aliphatic hydrocarbon chain,Ester, name is Ethyl 3-(dimethylamino)acrylate, and the molecular formula is C5H10N2OS, COA of Formula: C7H13NO2.

Zhu, Yun-fei published the artcileSynthesis of 5-amino-1-cyclopropyl-7-[3,5-dimethyl-1-piperazinyl]-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid (sparfloxacin), COA of Formula: C7H13NO2, the publication is Zhongguo Xinyao Zazhi (2008), 17(9), 757-759, database is CAplus.

A method for the synthesis of the title compound [i.e., 5-amino-1-cyclopropyl-7-(3,5-dimethyl-1-piperazinyl)-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, fluoroquinolone antibacterial agent] is reported here. Said compound was prepared from 2,3,4,5-tetrafluorobenzoic acid via nitration and acyl chlorination before coupling with Et (dimethylamino)acrylate, cyclopropylamine displacement, cyclization, reduction, hydrolysis and condensation with 2,6-dimethylpiperazine. The overall yield was 34.2%. Compared to a known process, this synthetic sequence eliminates three reaction steps; di-Et malonate condensation, partial hydrolysis decarboxylation and tri-Et orthoformate condensation. Said process has advantages, such as short reaction time, mild reaction conditions, waste reduction, yield increase, and a good prospect for industrial application.

Zhongguo Xinyao Zazhi published new progress about 924-99-2. 924-99-2 belongs to esters-buliding-blocks, auxiliary class Alkenyl,Amine,Aliphatic hydrocarbon chain,Ester, name is Ethyl 3-(dimethylamino)acrylate, and the molecular formula is C5H10N2OS, COA of Formula: C7H13NO2.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics

Wright, Jay S.’s team published research in Journal of the American Chemical Society in 143 | CAS: 757982-31-3

Journal of the American Chemical Society published new progress about 757982-31-3. 757982-31-3 belongs to esters-buliding-blocks, auxiliary class Boronic acid and ester,Boronic acid and ester, name is Methyl 4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate, and the molecular formula is C21H26Br4S2, Name: Methyl 4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate.

Wright, Jay S. published the artcileSequential Ir/Cu-Mediated Method for the Meta-Selective C-H Radiofluorination of (Hetero)Arenes, Name: Methyl 4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate, the publication is Journal of the American Chemical Society (2021), 143(18), 6915-6921, database is CAplus and MEDLINE.

This article describes a sequential Ir/Cu-mediated process for the meta-selective C-H radiofluorination of (hetero)arene substrates. In the first step, Ir-catalyzed C(sp2)-H borylation affords (hetero)aryl pinacolboronate (BPin) esters. The intermediate organoboronates are then directly subjected to copper-mediated radiofluorination with [18F]tetrabutylammonium fluoride to afford fluorine-18 labeled (hetero)arenes in high radiochem. yield and radiochem. purity. This entire process is performed on a bench top without Schlenk or glove box techniques and circumvents the need to isolate (hetero)aryl boronate esters. The reaction was automated on a TracerLab FXFN module with 1,3-dimethoxybenzene and a meta-tyrosine derivative The products, [18F]1-fluoro-3,5-dimethoxybenzene and an 18F-labeled meta-tyrosine derivative, were obtained in 37 ± 5% isolated radiochem. yield and >99% radiochem. purity and 25% isolated radiochem. yield and 99% radiochem. purity, and 0.52 Ci/μmol (19.24 GBq/μmol) molar activity (Am), resp.

Journal of the American Chemical Society published new progress about 757982-31-3. 757982-31-3 belongs to esters-buliding-blocks, auxiliary class Boronic acid and ester,Boronic acid and ester, name is Methyl 4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate, and the molecular formula is C21H26Br4S2, Name: Methyl 4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate.

Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics