Category: 93-97-0

Norman, DJ; Gambardella, A; Mount, AR; Murray, AF; Bradley, M in [Norman, Daniel J.; Gambardella, Alessia; Mount, Andrew R.; Bradley, Mark] Univ Edinburgh, EaStChem Sch Chem, David Brewster Rd, Edinburgh, Midlothian, Scotland; [Murray, Alan F.] Univ Edinburgh, Sch Engn, Mayfield Rd, Edinburgh, Midlothian, Scotland published A Dual Killing Strategy: Photocatalytic Generation of Singlet Oxygen with Concomitant Pt-IV Prodrug Activation in 2019, Cited 30. SDS of cas: 93-97-0. The Name is Benzoic anhydride. Through research, I have a further understanding and discovery of 93-97-0.

A ruthenium-based mitochondrial-targeting photosensitiser that undergoes efficient cell uptake, enables the rapid catalytic conversion of Pt-IV prodrugs into their active Pt-II counterparts, and drives the generation of singlet oxygen was designed. This dual mode of action drives two orthogonal cancer-cell killing mechanisms with temporal and spatial control. The designed photosensitiser was shown to elicit cell death of a panel of cancer cell lines including those showing oxaliplatin-resistance.

SDS of cas: 93-97-0. About Benzoic anhydride, If you have any questions, you can contact Norman, DJ; Gambardella, A; Mount, AR; Murray, AF; Bradley, M or concate me.

Reference:
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Keith, DJ; Townsend, SD in [Keith, D. Jamin; Townsend, Steven D.] Vanderbilt Univ, Dept Chem, 221 Kirkland Hall, Nashville, TN 37235 USA published Total Synthesis of the Congested, Bisphosphorylated Morganella morganii Zwitterionic Trisaccharide Repeating Unit in 2019, Cited 60. Name: Benzoic anhydride. The Name is Benzoic anhydride. Through research, I have a further understanding and discovery of 93-97-0.

Zwitterionic polysaccharides (ZPSs) activate T-cell-dependent immune responses by major histocompatibility complex class II presentation. Herein, we report the first synthesis of a Morganella morganii ZPS repeating unit as an enabling tool in the synthesis of novel ZPS materials. The repeating unit incorporates a 1,2-cis-alpha-glycosidic bond; the problematic 1,2-trans-galactosidic bond, Gal-beta-(1 -> 3)-GalNAc; and phosphoglycerol and phosphocholine residues which have not been previously observed together as functional groups on the same oligosaccharide. The successful third-generation approach leverages a first in class glycosylation of a phosphoglycerol-functionalized acceptor. To install the phosphocholine unit, a highly effective phosphocholine donor was synthesized.

Name: Benzoic anhydride. About Benzoic anhydride, If you have any questions, you can contact Keith, DJ; Townsend, SD or concate me.

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Authors Kamishima, T; Suzuki, M; Aoyagi, S; Watanabe, T; Koseki, Y; Kasai, H in PERGAMON-ELSEVIER SCIENCE LTD published article about PENTENOMYCIN-I; STEREOSELECTIVE-SYNTHESIS; EPIPENTENOMYCIN-I; CYCLOPENTENONE in [Kamishima, Takaaki; Watanabe, Toshihiro; Koseki, Yoshitaka; Kasai, Hitoshi] Tohoku Univ, Inst Multidisciplinary Res Adv Mat, Aoba Ku, 2-1-1 Katahira, Sendai, Miyagi 9808577, Japan; [Kamishima, Takaaki] Fromseeds Corp, Aoba Ku, 6-6-40 Aramaki, Sendai, Miyagi 9800845, Japan; [Suzuki, Masato] Natl Inst Infect Dis, Antimicrobial Resistance Res Ctr, 4-2-1 Aobamachi, Higashimurayama, Tokyo 1890002, Japan; [Aoyagi, Shigenobu] Ouchi Shinko Chem Ind Co Ltd, Res & Dev Ctr, 111 Shimojyukumae, Fukushima 9620806, Japan in 2019, Cited 27. Recommanded Product: Benzoic anhydride. The Name is Benzoic anhydride. Through research, I have a further understanding and discovery of 93-97-0

This study reported a stereoselective synthesis of (+)/(+)-pentenomycin I in 4-5 steps through regioselective silylation, optical resolution and dihydroxylation, followed by an olefin formation, from a known racemic cyclopentenone prepared from 2-deoxy-o-glucose. We also accomplished the transformation of a common intermediate into a variety of analogs. In addition, the antimicrobial activities of the pentenomycin analogs were evaluated, which revealed important structural factors of pentenomycins for the antimicrobial activities. (C) 2019 Elsevier Ltd. All rights reserved.

About Benzoic anhydride, If you have any questions, you can contact Kamishima, T; Suzuki, M; Aoyagi, S; Watanabe, T; Koseki, Y; Kasai, H or concate me.. Recommanded Product: Benzoic anhydride

Reference:
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Recently I am researching about 1ST TOTAL-SYNTHESIS; STEREOSELECTIVE-SYNTHESIS; NEURITOGENIC ACTIVITY; GANGLIOSIDE; ACID; FACILE; CONSTITUENTS; DERIVATIVES; CRINOIDEA; GLYCAN, Saw an article supported by the JSPS KAKENHI grantMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT)Japan Society for the Promotion of ScienceGrants-in-Aid for Scientific Research (KAKENHI) [JP18K05461, JP15K07409, JP15H04495, JP18H03942]; JST CREST Grant [JPMJCR18H2]; World Premier International Research Center Initiative the Institute of Integrated Cell-Material Sciences (WPI-iCeMS) from MEXT. Formula: C14H10O3. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Goto, K; Tamai, H; Takeda, Y; Tanaka, HN; Mizuno, T; Imamura, A; Ishida, H; Kiso, M; Ando, H. The CAS is 93-97-0. Through research, I have a further understanding and discovery of Benzoic anhydride

The first total synthesis of three echinodermatous sialyl inositol phosphosphingolipids, which exhibit unusual neuritogenic activity in the absence of nerve growth factor, are reported. Highlights of the syntheses include 9-O-methylation on sialic acid, inter-residual amide bond formation between sialic acid residues, and highly stereo- and regioselective sialylation of inositol. A key phosphodiester linkage between the mono-, di-, and trisialyl inositols and ceramide was formed at a late state employing the phosphoramidite method.

Formula: C14H10O3. About Benzoic anhydride, If you have any questions, you can contact Goto, K; Tamai, H; Takeda, Y; Tanaka, HN; Mizuno, T; Imamura, A; Ishida, H; Kiso, M; Ando, H or concate me.

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Recently I am researching about ASYMMETRIC CATALYSIS; COPPER(II) COMPLEXES; HYDROXYLATION; ACID; ESTERS; DESYMMETRIZATION; ENHANCEMENT; ISOLEUCINE; OXIDATION; VALINE, Saw an article supported by the EPFL (Switzerland); Swiss National Science FoundationSwiss National Science Foundation (SNSF)European Commission [SNSF 20020-155973]. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Wu, H; Andres, R; Wang, Q; Zhu, JP. The CAS is 93-97-0. Through research, I have a further understanding and discovery of Benzoic anhydride. SDS of cas: 93-97-0

A highly enantioselective alpha-ketol rearrangement has been developed. In the presence of a chiral Cu-bisoxazoline complex, achiral beta-hydroxy-alpha-dicarbonyls were isomerized to chiral alpha-hydroxy-beta-dicarbonyls and their bicyclic derivatives in excellent yields and enantioselectivities. Enantioenriched 2-acyl-2-hydroxy cyclohexan-1-ones, dihydroxyhexahydrobenzofuranones, and dihydroxyhexahydro-cycloheptafuranones, with up to three stereocenters, were readily prepared from achiral starting materials in one operation. The reaction is applicable to the desymmetrization of meso substrates and kinetic resolution of racemic alcohols.

About Benzoic anhydride, If you have any questions, you can contact Wu, H; Andres, R; Wang, Q; Zhu, JP or concate me.. SDS of cas: 93-97-0

Reference:
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,Isothiazole – ScienceDirect.com

Tolan, D; Almotairy, ARZ; Howe, O; Devereux, M; Montagner, D; Erxleben, A in [Tolan, Dina; Almotairy, Awatif Rashed Z.; Erxleben, Andrea] Natl Univ Ireland, Sch Chem, Galway, Ireland; [Almotairy, Awatif Rashed Z.; Howe, Orla; Devereux, Michael] Technol Univ Dublin, Sch Biol & Hlth Sci, City Campus, Dublin, Ireland; [Montagner, Diego] Maynooth Univ, Dept Chem, Maynooth, Kildare, Ireland; [Tolan, Dina] Menoufia Univ, Fac Sci, Dept Chem, Shibin Al Kawm, Egypt published Cytotoxicity and ROS production of novel Pt(IV) oxaliplatin derivatives with indole propionic acid in 2019, Cited 34. Computed Properties of C14H10O3. The Name is Benzoic anhydride. Through research, I have a further understanding and discovery of 93-97-0.

The coordination of biologically active moieties to the axial positions of Pt(IV) derivatives of Pt(II) anticancer drugs allows the co-delivery and simultaneous activation of two pro-drugs for combination therapy. Pt(IV) complexes with a redox modulator as an axial ligand can kill cancer cells by a mechanism combining DNA platination and generation of oxidative stress. In this study we evaluated the cytotoxicity of Pt(IV) complexes based on the oxaliplatin scaffold and the pro-oxidant indole-3-propionate in cisplatin-sensitive and cisplatin-resistant ovarian cancer cells. A series of five complexes was synthesized and characterized by H-1 and Pt-195 NMR spectroscopy, IR spectroscopy, mass spectrometry and elemental analysis; trans-[Pt(DACH)(ox)(IPA)(OH)] (1), trans-[Pt(DACH)(ox)(IPA)(2)] (2), trans-[Pt(DACH)(ox)(IPA)(bz)] (3), trans-[Pt(DACH)(ox)(IPA)(suc)] (4), and trans-[Pt(DACH)(ox)(IPA)(ac)] (5) (DACH = 1,2-diaminocyclohexane (1R, 2R)-(-), ox = oxalate, IPA = indole 3-propionate, bz = benzoate, suc = succinate and ac = acetate). The complexes were shown to produce cellular reactive oxygen species (ROS) in a time-dependent manner. The most potent ROS producer, complex 1, also elicited the highest cytotoxicity. Complex 1 was shown to form the mono-and bis-adducts [Pt(DACH)(guanosine)( OH)](+) and [Pt(DACH)(guanosine)(2)](2+) in the presence of ascorbic acid, suggesting that on activation the released oxaliplatin will interact with DNA.

About Benzoic anhydride, If you have any questions, you can contact Tolan, D; Almotairy, ARZ; Howe, O; Devereux, M; Montagner, D; Erxleben, A or concate me.. Computed Properties of C14H10O3

Reference:
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,Isothiazole – ScienceDirect.com

Quality Control of Benzoic anhydride. Authors Kostopoulos, N; Banse, F; Fave, C; Anxolabehere-Mallart, E in ROYAL SOC CHEMISTRY published article about in [Kostopoulos, Nikolaos; Fave, Claire; Anxolabehere-Mallart, Elodie] Univ Paris, Lab Electrochim Mol, UMR 7591, CNRS, F-75013 Paris, France; [Banse, Frederic] Univ Paris Saclay, CNRS, Inst Chim Mol & Mat Orsay, F-91405 Orsay, France in 2021, Cited 22. The Name is Benzoic anhydride. Through research, I have a further understanding and discovery of 93-97-0

Oxidation of organic substrates is achieved in nature under mild conditions thanks to metalloenzymes but remains a challenge for chemists. Herein we show by UV-Vis spectroelectrochemistry that when (MnTPPCl)-T-III is electrochemically reduced to Mn-II in CH2Cl2 under O-2, a (MnO2)-O-II species is generated. Benzoic anhydride reacts with the latter triggering a catalytic current in cyclic voltammetry. Electrolysis on the catalytic wave in the presence of cyclooctene leads to its oxygenation or halogenation depending on the axial ligand present as reported here for the first time.

About Benzoic anhydride, If you have any questions, you can contact Kostopoulos, N; Banse, F; Fave, C; Anxolabehere-Mallart, E or concate me.. Quality Control of Benzoic anhydride

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An article Structure-activity relationship of 4-azaindole-2-piperidine derivatives as agents against Trypanosoma cruzi WOS:000499694600015 published article about CHAGAS-DISEASE; RANDOMIZED-TRIAL; TRANSMISSION; BENZNIDAZOLE in [Koovits, Paul J.; Dessoy, Marco A.; Dias, Luiz C.] Univ Estadual Campinas, UNICAMP, Inst Chem, Rua Josue Castro S-N,Cidade Univ, BR-13083861 Campinas, SP, Brazil; [Matheeussen, An; Maes, Louis; Caljon, Guy] LMPH, Univ Pl 1, B-2610 Antwerp, Belgium; [Mowbray, Charles E.; Kratz, Jadel M.] DNDi, 15 Chemin Louis Dunant, CH-1202 Geneva, Switzerland in 2020, Cited 21. The Name is Benzoic anhydride. Through research, I have a further understanding and discovery of 93-97-0. Formula: C14H10O3

The structure-activity relationship of a 4-Azaindole-2-piperidine compound selected from GlaxoSmithKline’s recently disclosed open-resource Chagas box and possessing moderate activity against Trypanosoma cruzi, the parasite responsible for Chagas disease, is presented. Despite considerable medicinal chemistry efforts, a suitably potent and metabolically stable compound could not be identified to advance the series into in vivo studies. This research should be of interest to those in the area of neglected diseases and in particular anti-kinetoplastid drug discovery.

Formula: C14H10O3. About Benzoic anhydride, If you have any questions, you can contact Koovits, PJ; Dessoy, MA; Matheeussen, A; Maes, L; Caljon, G; Mowbray, CE; Kratz, JM; Dias, LC or concate me.

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In 2019 GREEN CHEM published article about CHEMISTRY RESEARCH AREAS; GREEN CHEMISTRY; BOND FORMATION; CARBOXYLIC-ACIDS; AMINES; ALCOHOLS; PERSPECTIVE; AMIDATION; WATER in [Dissanayake, D. M. M. Mevan; Melville, Alex D.; Vannucci, Aaron K.] Univ South Carolina, Dept Chem & Biochem, Columbia, SC 29208 USA in 2019, Cited 33. The Name is Benzoic anhydride. Through research, I have a further understanding and discovery of 93-97-0. Formula: C14H10O3

An electrosynthesis method for amide bond formation has been developed in an attempt to increase the atom economy for this class of reactions. This anion pool method electrochemically generates strong nucleophiles from amine substrates. The amine nucleophiles then react with acid anhydrides to generate amides, and the by- product from this reaction undergoes further chemical transformations to generate pharmaceutically relevant benzoic esters. These one- pot reactions are operationally simple, are performed at room temperature, and avoid rare transition metals and added bases. The amide synthesis is amenable to primary and secondary amines and a variety of anhydrides with yields up to 90% obtained. Atom economy and process mass index ( PMI) values calculated for this procedure indicate that this process can be considered greener compared to traditional amide synthesis routes used by industry. Furthermore, this electrochemical approach showed unique selectivity when substrates that contained two inequivalent amine moieties were examined.

About Benzoic anhydride, If you have any questions, you can contact Dissanayake, DMMM; Melville, AD; Vannucci, AK or concate me.. Formula: C14H10O3

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COA of Formula: C14H10O3. Zheng, XM; Liu, S; Rehman, S; Li, ZH; Zhang, PY in [Zheng, Xianming; Liu, Shuai; Rehman, Sadia; Li, Zehui; Zhang, Pengyi] Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Con, Beijing 100084, Peoples R China; [Zhang, Pengyi] Beijing Key Lab Indoor Air Qual Evaluat & Control, Beijing 100084, Peoples R China published Highly improved adsorption performance of metal-organic frameworks CAU-1 for trace toluene in humid air via sequential internal and external surface modification in 2020, Cited 46. The Name is Benzoic anhydride. Through research, I have a further understanding and discovery of 93-97-0.

Trace volatile organic compounds (VOCs) such as aldehydes and aromatics significantly deteriorate the indoor air quality especially in newly-decorated buildings. The universal water vapor would greatly decrease the adsorption capacity of ad-sorbents for trace VOCs via competitive adsorption and capillary condensation. Herein, we developed a strategy to subsequently modify the internal and external surface of CAU-1, an aluminum-based metal-organic framework (MOF), to significantly improve its humidity resistance. First, anhydrides were used to transfer amino groups of CAU-1 into hydrophobic groups via amide reaction. Second, polydimethylsiloxane was used to form a hydorphobic coating on its external surface. The adsorption capacity of as-modified CAU-1 for 1 ppm toluene increased about 6 times under 50% relative humidity (RH) at 298 K, even much higher than those of common adsorbents including hydrophobic ZSM-5. In addition, it could be completely regenerated below 373 K, about 65 K lower than that required for regenerating ZSM-5 under the same condition, which not only greatly reduces the energy consumption but also improves the safety and feasibility of in-situ regeneration of adsorbents in indoor environment.

About Benzoic anhydride, If you have any questions, you can contact Zheng, XM; Liu, S; Rehman, S; Li, ZH; Zhang, PY or concate me.. COA of Formula: C14H10O3

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com