Month: October 2021

An article Self-assembly pattern directed sustained release from porous microspheres of discotic tripeptides WOS:000625321000047 published article about IRON-OXIDE NANOPARTICLES; CARBON NANOTUBES; DRUG-DELIVERY; PEPTIDE; NANOVESICLES; STABILIZATION; NANOCARRIERS; FABRICATION; DENDRIMERS; POLYMERS in [Kumar, Santosh; Bera, Santu; Nandi, Sujay Kumar; Haldar, Debasish] Indian Inst Sci Educ & Res Kolkata, Dept Chem Sci, Mohanpur 741246, W Bengal, India in 2020, Cited 73. COA of Formula: C10H11NO4. The Name is Dimethyl 5-aminoisophthalate. Through research, I have a further understanding and discovery of 99-27-4

Porous microspheres from discotic tripeptides have been investigated as potential candidates for drug delivery vehicles. The C-3 symmetric discotic tripeptide adopts a supramolecular helical column structure by three fold intermolecular hydrogen bonding interactions as well as face to face pi-pi stacking interactions. But the C-2 symmetric discotic tripeptide adopts a supramolecular dimer like structure by six-fold intermolecular hydrogen bonding interactions and face to face pi-pi stacking interactions. Field emission scanning electron microscopy (FE-SEM) revealed that the C-3 symmetric discotic tripeptide exhibits bird nest-like porous microsphere morphology formed by the assembly of the individual columns. However the C-2 symmetric discotic tripeptide forms round clay pitcher like porous microspheres. These porous microspheres have been used as potential carriers for the sustained release of a bacteriostatic antibiotic sulfamethoxazole. The spectroscopic studies as well as the growth inhibition of E. coli reveal that the round clay pitcher-like porous microspheres are more efficient than the bird nest-like porous microspheres for the sustained release of drugs. The report highlights the importance of the self-assembly pattern for the fabrication of advanced functional materials.

COA of Formula: C10H11NO4. About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Kumar, S; Bera, S; Nandi, SK; Haldar, D or concate me.

Reference:
Patent; ASTRA ZENECA AB; NPS PHARMACEUTICALS, INC.; WO2004/14881; (2004); A2;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Name: 6H-Benzo[c]chromen-6-one. In 2020.0 J AM CHEM SOC published article about METAL CHARGE-TRANSFER; VISIBLE-LIGHT; PHOTOREDOX CATALYSIS; DEHYDROGENATIVE LACTONIZATION; EFFECTIVE ALKYLATION; GAMMA-LACTONES; PYRIDINE RING; COMPLEXES; FUNCTIONALIZATION; CYCLIZATION in [Shirase, Satoru; Tamaki, Sota; Shinohara, Koichi; Tsurugi, Hayato; Mashima, Kazushi] Osaka Univ, Grad Sch Engn Sci, Dept Chem, Toyonaka, Osaka 5608531, Japan; [Hirosawa, Keishi; Satoh, Tetsuya] Osaka City Univ, Grad Sch Sci, Dept Chem, Osaka 5588585, Japan in 2020.0, Cited 56.0. The Name is 6H-Benzo[c]chromen-6-one. Through research, I have a further understanding and discovery of 2005-10-9.

We found that in situ generated cerium(IV) carboxylate generated by mixing the precursor Ce((OBu)-Bu-t)(4) with the corresponding carboxylic acids served as efficient photocatalysts for the direct formation of carboxyl radicals from carboxylic acids under blue light-emitting diodes (blue LEDs) irradiation and air, resulting in catalytic decarboxylative oxygenation of aliphatic carboxylic acids to give C-O bond-forming products such as aldehydes and ketones. Control experiments revealed that hexanuclear Ce(IV) carboxylate clusters initially formed in the reaction mixture and the ligand-to-metal charge transfer nature of the Ce(IV) carboxylate clusters was responsible for the high catalytic performance to transform the carboxylate ligands to the carboxyl radical. In addition, the Ce(IV) carboxylate cluster catalyzed direct lactonization of 2-isopropylbenzoic acid to produce the corresponding peroxy lactone and gamma-lactone via intramolecular 1,5-hydrogen atom transfer (1,5-HAT).

Name: 6H-Benzo[c]chromen-6-one. About 6H-Benzo[c]chromen-6-one, If you have any questions, you can contact Shirase, S; Tamaki, S; Shinohara, K; Hirosawa, K; Tsurugi, H; Satoh, T; Mashima, K or concate me.

Reference:
Article; Zhang, Jian; Shi, Dongdong; Zhang, Haifeng; Xu, Zheng; Bao, Hanyang; Jin, Hongwei; Liu, Yunkui; Tetrahedron; vol. 73; 2; (2017); p. 154 – 163;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

An article Intramolecular Aromatic C-H Acyloxylation Enabled by Iron Photocatalysis WOS:000516667200032 published article about DEHYDROGENATIVE LACTONIZATION; PHOTOREDOX CATALYSIS; CARBOXYLIC-ACIDS; METAL-COMPLEXES; C(SP(2))-H; FUNCTIONALIZATION; DIBENZOPYRANONES; LACTONES; SYSTEM in [Xia, Siqi; Lei, Chuanhu] Shanghai Univ, Coll Sci, Ctr Supramol Chem & Catalysis, Shanghai 200444, Peoples R China; [Xia, Siqi; Lei, Chuanhu] Shanghai Univ, Coll Sci, Dept Chem, Shanghai 200444, Peoples R China; [Xia, Siqi; Hu, Kunjun; Jin, Jian] Chinese Acad Sci, Univ Chinese Acad Sci, Shanghai Inst Organ Chem, CAS Key Lab Synthet Chem Nat Subst,Ctr Excellence, Shanghai 20032, Peoples R China in 2020.0, Cited 73.0. The Name is 6H-Benzo[c]chromen-6-one. Through research, I have a further understanding and discovery of 2005-10-9. Computed Properties of C13H8O2

A mild and efficient protocol for the intramolecular aromatic C-H oxygenation of 2-biphenylcarboxylic acids has been achieved via iron photocatalysis. The 2-biphenylcarboxylic acids with a diverse array of substituents at both phenyl rings could furnish the oxygenation products in good to excellent yields. We speculate that the aryl carboxylate-iron(III) complexes should generate the aroyloxy radicals and iron(II) upon visible light irradiation.

About 6H-Benzo[c]chromen-6-one, If you have any questions, you can contact Xia, SQ; Hu, KJ; Lei, CH; Jin, J or concate me.. Computed Properties of C13H8O2

Reference:
Article; Zhang, Jian; Shi, Dongdong; Zhang, Haifeng; Xu, Zheng; Bao, Hanyang; Jin, Hongwei; Liu, Yunkui; Tetrahedron; vol. 73; 2; (2017); p. 154 – 163;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Authors Urruzuno, I; Mugica, O; Zanella, G; Vera, S; Gomez-Bengoa, E; Oiarbide, M; Palomo, C in WILEY-V C H VERLAG GMBH published article about VINYLOGOUS ALDOL REACTION; ORGANOCATALYTIC MICHAEL ADDITION; MANNICH-TYPE REACTIONS; DIELS-ALDER REACTION; ALLYL ARYL KETONES; ASYMMETRIC-SYNTHESIS; GAMMA-BUTENOLIDES; CYCLIC-KETONES; ALPHA,BETA-UNSATURATED ALDEHYDES; 3-ALKYLIDENE OXINDOLES in [Urruzuno, Inaki; Mugica, Odei; Zanella, Giovanna; Vera, Silvia; Gomez-Bengoa, Enrique; Oiarbide, Mikel; Palomo, Claudio] Univ Pais Vasco UPV EHU, Dept Quim Organ 1, Manuel Lardizabal 3, San Sebastian 20018, Spain in 2019, Cited 137. Application In Synthesis of Dimethyl 5-aminoisophthalate. The Name is Dimethyl 5-aminoisophthalate. Through research, I have a further understanding and discovery of 99-27-4

In this study, the unique capacity of bifunctional BrOnsted bases to generate alpha-branched ketone dienolates and control both site- and stereoselectivity of their addition reactions to representative classes of carbon electrophiles (i.e., vinyl sulfones, nitroolefins, formaldehyde) is documented. We demonstrate that by using selected chiral tertiary amine/squaramide catalysts, the reactions of beta,gamma-unsaturated cycloalkanones proceed through the dienolate C alpha almost exclusively and provide all-carbon quaternary cyclic ketone adducts in good yields with very high enantioselectivities. A minor amount (<5%) of gamma-addition is observed when nitroolefins are used as electrophiles. The parent acyclic ketone dienolates proved to be less reactive under these conditions, and thus still constitute a challenging class of substrates. Quantum chemical calculations correctly predict these differences in reactivity and explain the observed site-specificity and enantioselectivity. About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Urruzuno, I; Mugica, O; Zanella, G; Vera, S; Gomez-Bengoa, E; Oiarbide, M; Palomo, C or concate me.. Application In Synthesis of Dimethyl 5-aminoisophthalate

Reference:
Patent; ASTRA ZENECA AB; NPS PHARMACEUTICALS, INC.; WO2004/14881; (2004); A2;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

An article N-Substituted Benzene-1-Urea-3,5-Biscarboxamide (BUBA): Easily Accessible C-2-Symmetric Monomers for the Construction of Reversible and Chirally Amplified Helical Assemblies WOS:000476852100001 published article about SUPRAMOLECULAR POLYMERS; AMPLIFICATION; POLYMERIZATION; BENZENE-1,3,5-TRICARBOXAMIDES; ARCHITECTURES; RULES; NANOPARTICLES; DERIVATIVES; STABILITY; PRINCIPLE in [Li, Yan; Dubreucq, Ludovic; Alvarenga, Bruno G.; Raynal, Matthieu; Bouteiller, Laurent] Sorbonne Univ, CNRS, Inst Parisien Chim Mol, Equipe Chim Polymeres, 4 Pl Jussieu, F-75005 Paris, France; [Alvarenga, Bruno G.] Univ Estadual Campinas, UNICAMP, Dept Phys Chem, Inst Chem, Campinas, SP, Brazil in 2019, Cited 85. SDS of cas: 99-27-4. The Name is Dimethyl 5-aminoisophthalate. Through research, I have a further understanding and discovery of 99-27-4

Non-C-3-symmetric supramolecular helices are gaining interest for the design of hierarchical assemblies, for the compartmentalisation or the self-assembly of polymer chains and for application in asymmetric catalysis. Herein, N-substituted benzene-1-urea-3,5-biscarboxamide (BUBA) monomers, which consist of one urea and two carbon-connected amide functions linked to an aromatic ring, are introduced as an easily accessible class of C-2-symmetric supramolecular synthons. In apolar solvents, BUBA monomers assemble into long helical assemblies by means of hydrogen-bonding and aromatic interactions, as assessed by several analytical techniques. To probe the influence of the urea function, BUBA and related benzene-1,3,5-tricarboxamide (BTA) helical polymers have been compared, in terms of their thermodynamics of formation, stability, reversibility and chiral amplification properties. Similar to BTA, BUBA monomers form long helices reversibly through a highly cooperative mechanism and the helicity of their assemblies is governed by chiral amplification effects. However, precise quantification of their properties reveals that BUBA monomers assemble in a more cooperative manner. Also, chiral amplification operates to a higher extent in BUBA helices, as probed by both sergeants-and-soldiers and majority-rules experiments. Compatibility between urea and amide functions also allows the formation of co-assemblies that incorporate both BUBA and BTA monomers. Importantly, a small amount of chiral BUBA monomers in these co-assemblies is sufficient to obtain single-handed helices; thus paving the way towards the development of functional supramolecular helices.

SDS of cas: 99-27-4. About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Li, Y; Dubreucq, L; Alvarenga, BG; Raynal, M; Bouteiller, L or concate me.

Reference:
Patent; ASTRA ZENECA AB; NPS PHARMACEUTICALS, INC.; WO2004/14881; (2004); A2;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Wadekar, K; Aswale, S; Yatham, VR in [Wadekar, Ketan] CSIR IICT, Hyderabad, Telangana, India; [Wadekar, Ketan] Acad Sci & Innovat Res AcSIR, Ghaziabad, India; [Aswale, Suraj; Yatham, Veera Reddy] CSIR IICT, Dept Organ Synth & Proc Chem, Hyderabad 500007, Telangana, India published Cerium photocatalyzed dehydrogenative lactonization of 2-arylbenzoic acids in 2020.0, Cited 67.0. Category: esters-buliding-blocks. The Name is 6H-Benzo[c]chromen-6-one. Through research, I have a further understanding and discovery of 2005-10-9.

The first cerium photocatalyzed dehydrogenative lactonization of 2-arylbenzoic acids has been developed. This operationally simple protocol allows rapid access to synthetically useful coumarins on gram scale by employing CeCl3 as a photocatalyst and O-2 as a terminal oxidant. Overall, this delivers an economical and environmentally amiable entry to diversely substituted coumarins, important structural motifs in bioactive molecules.

Category: esters-buliding-blocks. About 6H-Benzo[c]chromen-6-one, If you have any questions, you can contact Wadekar, K; Aswale, S; Yatham, VR or concate me.

Reference:
Article; Zhang, Jian; Shi, Dongdong; Zhang, Haifeng; Xu, Zheng; Bao, Hanyang; Jin, Hongwei; Liu, Yunkui; Tetrahedron; vol. 73; 2; (2017); p. 154 – 163;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

COA of Formula: C10H11NO4. In 2020 CRYST GROWTH DES published article about SELECTIVE DETECTION; NITROAROMATIC EXPLOSIVES; GAS-ADSORPTION; QUANTUM DOTS; ACID; ANTIBIOTICS; DENDRIMERS; MOLECULE; POLYMER; SENSORS in [Zhang, Meng-Yun; Dai, Ru-Dan; Li, Bang-Jian; Hang, Tian-Xiang; Xie, Jia-Xin; Zhu, Xian-Dong] Anhui Polytech Univ, Coll Biol & Chem Engn, Wuhu 241000, Peoples R China; [Lu, Jian; Zhu, Xian-Dong] Chinese Acad Sci, Fujian Inst Res Struct Matter, Fuzhou 350002, Peoples R China; [Lu, Jian] Fujian Agr & Forestry Univ, Coll Resources & Environm, Fujian Prov Key Lab Soil Environm Hlth & Regulat, Fuzhou 350002, Peoples R China in 2020, Cited 34. The Name is Dimethyl 5-aminoisophthalate. Through research, I have a further understanding and discovery of 99-27-4.

A Cd(II)-based metal-organic framework as fluorescent chemical sensor, formulated as {[Cd-3(bmipia)(2)]center dot 10DMF center dot 5H(2)O}(n) (FCS-2), was synthesized through a hydrothermal process and structurally characterized via X-ray crystallography. FCS-2 represented a new three-dimensional framework assembled from a semi -rigid aromatic carboxylate ligand and exhibited fascinating fluorescence due to the highly crystalline and ordered molecular structure. The emission of FCS-2 could be quenched, interestingly, by the presence of trace 2,4,6-trinitrophenol, which indicated that FCS-2 can be applied as a potentially sensitive fluorescent chemical sensor for the detection of nitroaromatic compounds.

COA of Formula: C10H11NO4. About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Zhang, MY; Dai, RD; Li, BJ; Hang, TX; Xie, JX; Lu, J; Zhu, XD or concate me.

Reference:
Patent; ASTRA ZENECA AB; NPS PHARMACEUTICALS, INC.; WO2004/14881; (2004); A2;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Recommanded Product: Dimethyl 5-aminoisophthalate. Recently I am researching about FLAME-RETARDANT; EPOXY; NETWORKS; THERMO; POLYURETHANE; DEGRADATION; PYROLYSIS; MALEIMIDE; MECHANISM; STRATEGY, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21634006, 51827803, 51721091]; Sichuan Province Youth Science and Technology Innovation Team [2017TD0006]. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Chen, L; Zhao, HB; Ni, YP; Fu, T; Wu, WS; Wang, XL; Wang, YZ. The CAS is 99-27-4. Through research, I have a further understanding and discovery of Dimethyl 5-aminoisophthalate

The practical problems of insufficient mechanical strength, poor processability, tedious synthesis and flammability facing shape memory polymers have limited their further usage in industrial fields, especially in construction and aerospace. A novel and very simple method of ternary polymerization is presented here to prepare multi-functional copolyesters from general poly(ethylene terephthalate) (PET) through the new well-designed third monomer that features pendent phenylacetylene-phenylimide units. The pi-pi stacking between phenylacetylene groups as a reversible net-point not only endows the copolyesters with good shape memory and self-healability, but also reinforces the interchain interaction, leading to high tensile strength (79.6-89.6 MPa). Interestingly enough, the phenylacetylene can synergistically crosslink with the unsaturated C N group generated from the phenylimide during burning, resulting in excellent flame retardancy. Thermoplastic smart copolyesters can be designed into fire alarms and can also be used for 3D printing. The printed geometries exhibit good shape memory behaviors, which could be deformed into a small size to save space during transportation/storage and allow manufacturing freedom for space applications.

About Dimethyl 5-aminoisophthalate, If you have any questions, you can contact Chen, L; Zhao, HB; Ni, YP; Fu, T; Wu, WS; Wang, XL; Wang, YZ or concate me.. Recommanded Product: Dimethyl 5-aminoisophthalate

Reference:
Patent; ASTRA ZENECA AB; NPS PHARMACEUTICALS, INC.; WO2004/14881; (2004); A2;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

An article Supercritical CO2 extraction and selective adsorption of aroma materials of selected spice plants in functionalized silica aerogels WOS:000465053500003 published article about FLUID EXTRACTION; ESSENTIAL OIL in [Gyori, Eniko; Varga, Anita; Fabian, Istvan; Lazar, Istvan] Univ Debrecen, Dept Inorgan & Analyt Chem, Egyet Ter 1, H-4032 Debrecen, Hungary; [Fabian, Istvan; Lazar, Istvan] Univ Debrecen, MTA DE Redox & Homogeneous Catalyt React Mech Res, Egyet Ter 1, H-4032 Debrecen, Hungary in 2019.0, Cited 31.0. Name: Methyl 3-phenyl-2-propenoate. The Name is Methyl 3-phenyl-2-propenoate. Through research, I have a further understanding and discovery of 103-26-4

Static supercritical fluid extraction has been used to concentrate the aroma materials of common herbs and spices. The technique has provided a higher number of components and cleaner extract than the one-step ethanol maceration. The one-step supercritical fluid extraction of the aroma compounds has been combined with their in situ adsorption in hydrophilic and hydrophobic silica aerogels. The extracts have been analyzed by a GC-MS technique and 55 aroma compounds have been identified. Most of the compounds have been adsorbed in both polar and apolar silica aerogels with no direct connection with the surface polarity. However, previously undetected compounds enriched to an analytically significant level, while others competed with each other for the active sites on the surface. Functionalized silica aerogels can be used as a new type of aroma storage materials and as selective and tuneable adsorbents for the extraction and enrichment of potentially active components from a complex matrix.

About Methyl 3-phenyl-2-propenoate, If you have any questions, you can contact Gyori, E; Varga, A; Fabian, I; Lazar, I or concate me.. Name: Methyl 3-phenyl-2-propenoate

Reference:
Article; Weng, Shiue-Shien; Ke, Chih-Shueh; Chen, Fong-Kuang; Lyu, You-Fu; Lin, Guan-Ying; Tetrahedron; vol. 67; 9; (2011); p. 1640 – 1648;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Recently I am researching about TANDEM WESSELY OXIDATION; CYCLOADDITION; ALKALOIDS; ADDITIONS, Saw an article supported by the JSPS KAKENHIMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT)Japan Society for the Promotion of ScienceGrants-in-Aid for Scientific Research (KAKENHI) [JP19K05473]; Kanazawa University SAKIGAKE project. Recommanded Product: 2005-10-9. Published in PHARMACEUTICAL SOC JAPAN in TOKYO ,Authors: Hanashima, M; Matsumura, T; Asaji, Y; Yoshimura, T; Matsuo, J. The CAS is 2005-10-9. Through research, I have a further understanding and discovery of 6H-Benzo[c]chromen-6-one

Regioselectivity for intramolecular Diels-Alder (IMDA) reactions of 6-acetoxy-6-alkenylcyclohexa-2,4-dien-1-ones that were formed by oxidation of 2-alkenylphenols with lead tetraacetate in acetic acid were studied. Bridged regioselectivity was observed in the IMDA reactions of 6-acetoxy-6-alkenylcyclohexa-2,4-dien-1-ones having a dienophile part which could conjugate with an aromatic group. Bridged seven-and eight-membered rings and bicyclo[2.2.2]octane skeletons were constructed by the present IMDA reactions. Density functional theory (DFT) calculations suggested that conjugation of the dienophile with neighboring aromatic groups lowered the highest occupied molecular orbital-lowest unoccupied molecular orbital (HOMO-LUMO) energy gap and preceded bridged [4 + 2] adducts.

Recommanded Product: 2005-10-9. About 6H-Benzo[c]chromen-6-one, If you have any questions, you can contact Hanashima, M; Matsumura, T; Asaji, Y; Yoshimura, T; Matsuo, J or concate me.

Reference:
Article; Zhang, Jian; Shi, Dongdong; Zhang, Haifeng; Xu, Zheng; Bao, Hanyang; Jin, Hongwei; Liu, Yunkui; Tetrahedron; vol. 73; 2; (2017); p. 154 – 163;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics