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Recommanded Product: 99-04-7. In 2020 BIOORG MED CHEM LETT published article about HISTONE DEACETYLASE INHIBITORS; 4-PHENOXYQUINOLINE DERIVATIVES; MULTITARGET THERAPEUTICS; MULTIPLE LIGANDS; CANCER; MET; POLYPHARMACOLOGY; RECEPTOR; MOIETY in [Dong, Yuhong; Hu, Hao; Sun, Yuwei; Qin, Mingze; Gong, Ping; Hou, Yunlei; Zhao, Yanfang] Shenyang Pharmaceut Univ, Key Lab Struct Based Drug Design & Discovery, Minist Educ, 103 Wenhua Rd, Shenyang 110016, Peoples R China in 2020, Cited 29. The Name is 3-Methylbenzoic acid. Through research, I have a further understanding and discovery of 99-04-7.

In this work three novel series of c-Met/HDAC bifunctional inhibitors were designed and synthesized by merging pharmacophores of c-Met and HDAC inhibitors. The most potent compound 11j inhibited c-Met kinase and HDAC1 with IC50 values of 21.44 and 45.22 nM, respectively. In addition, 11j showed efficient antiproliferative activities against both MCF-7 and A549 cells with greater potency than the reference drug SAHA and Cabozantinib. This work may lay the foundation for developing novel dual c-Met/HDAC inhibitors as potential anticancer therapeutics.

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Category: isothiazole. In 2019 ACS CATAL published article about C BOND FORMATION; TRACELESS DIRECTING GROUPS; H ARYLATION; BENZOIC-ACIDS; ARYL; CYCLIZATION; ALKYNES; BETA; HYDROARYLATION; CONDENSATION in [Zhang, Guodong; Hu, Zhiyong; Bertoli, Giulia; Goossen, Lukas J.] Ruhr Univ Bochum, Fak Chem & Biochem, Univ Str 150, D-44801 Bochum, Germany in 2019, Cited 67. The Name is 3-Methylbenzoic acid. Through research, I have a further understanding and discovery of 99-04-7.

A catalytic annulation is presented that provides straightforward, modular synthetic access to 3-substituted indanones from benzoic acids and alpha,beta-unsaturated ketones. It is catalyzed by a bimetallic Ir/In system and proceeds via hydroarylation followed by Claisen condensation and optional retro-Claisen deacylation. The annulation may be combined into a one-pot procedure with the synthesis of the unsaturated ketone substrates from aldehydes and acetone. Two complementary reaction protocols are provided that are applicable to diversely functionalized electron-rich and electron-poor substrates.

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Tao, N; Wang, J; Yuan, CC; Zeng, RS; Zhao, YS in [Tao, Na; Wang, Jie; Yuan, Chunchen; Zeng, Runsheng; Zhao, Ying-Sheng] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Key Lab Organ Synth Jiangsu Prov, Suzhou 215123, Peoples R China published Palladium-Catalyzed Carboxylate-Assisted Ethoxycarboxylation of Aromatic Acids To Synthesize Monoethyl Phthalate Derivatives with Ethyl Bromodifluoroacetate in 2019.0, Cited 34.0. Name: 3-Methylbenzoic acid. The Name is 3-Methylbenzoic acid. Through research, I have a further understanding and discovery of 99-04-7.

A novel and efficient approach for direct carbonation of aromatic acids with ethyl bromodifluoroacetate as the carbonyl source is reported. A broad range of substrates bearing various functional groups were tolerated, leading to monoalkyl phthalate derivatives in moderate to good yields.

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Application In Synthesis of 3-Methylbenzoic acid. Welcome to talk about 99-04-7, If you have any questions, you can contact Honjo, Y; Shibata, Y; Tanaka, K or send Email.

I found the field of Chemistry very interesting. Saw the article Rhodium-Catalyzed [2+1+2+1] Cycloaddition of Benzoic Acids with Diynes through Decarboxylation and C equivalent to C Triple Bond Cleavage published in 2019. Application In Synthesis of 3-Methylbenzoic acid, Reprint Addresses Shibata, Y; Tanaka, K (corresponding author), Tokyo Inst Technol, Dept Chem Sci & Engn, Meguro Ku, Tokyo 1528550, Japan.. The CAS is 99-04-7. Through research, I have a further understanding and discovery of 3-Methylbenzoic acid

It has been established that an electron-deficient cyclopentadienyl rhodium(III) ((CpRhIII)-Rh-E) complex catalyzes the oxidative and decarboxylative [2+1+2+1] cycloaddition of benzoic acids with diynes through C equivalent to C triple bond cleavage, leading to fused naphthalenes. This cyclotrimerization is initiated by directed ortho C-H bond cleavage of a benzoic acid, and the subsequent regioselective alkyne insertion and decarboxylation produce a five-membered rhodacycle. The electron-deficient nature of the (CpRhIII)-Rh-E complex promotes reductive elimination giving a cyclobutadiene-rhodium(I) complex rather than the second intermolecular alkyne insertion. The oxidative addition of the thus generated cyclobutadiene to rhodium(I) (formal C equivalent to C triple bond cleavage) followed by the second intramolecular alkyne insertion and reductive elimination give the corresponding [2+1+2+1] cycloaddition product. The synthetic utility of the present [2+1+2+1] cycloaddition was demonstrated in the facile synthesis of a donor-acceptor [5]helicene and a hemi-hexabenzocoronene by a combination with the chemoselective Scholl reaction.

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Recommanded Product: 99-04-7. Recently I am researching about ABUNDANT METAL-CATALYSTS; SELECTIVE OXIDATION; CARBOXYLIC-ACIDS; C-H; DEHYDROGENATIVE OXIDATION; PROMOTED OXIDATION; AEROBIC OXIDATION; ORGANIC-REACTIONS; GREEN CHEMISTRY; EARTH, Saw an article supported by the DST, IndiaDepartment of Science & Technology (India) [DST EMR/2015/000285]; UGC, IndiaUniversity Grants Commission, India; DST-FISTDepartment of Science & Technology (India); IIT D. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Hazra, S; Kushawaha, AK; Yadav, D; Dolui, P; Deb, M; Elias, AJ. The CAS is 99-04-7. Through research, I have a further understanding and discovery of 3-Methylbenzoic acid

A simple, efficient, sustainable and economical method for the oxidation of alcohols and amines has been developed based on chloride, a sea abundant anionic catalyst for the practical synthesis of a wide range of carboxylic acids, ketones and imines. Oxidation of aromatic alcohols was carried out using NaCl (20 mol%) as the catalyst, NaOH (50 mol%) and aq. TBHP (4 equiv.) as the oxidant in 55-92% isolated yields. Oxidation of aromatic amines to imines was achieved by using only 20 mol% of NaCl and aq. TBHP (4 equiv.) in 32-93% isolated yields. The chlorine species formed during the reaction as the active oxidation catalyst has been identified as ClO2- for alcohols and ClO-/ClO2- for amines by control experiments. This method is mostly free from chromatographic purification, which makes it suitable for large-scale synthesis. We have scaled up to 30 gram scale the synthesis of carboxylic acids and imines in good yields and have also carried out efficiently this new method using filtered sea water as the solvent and catalyst.

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Welcome to talk about 99-04-7, If you have any questions, you can contact Emayavaramban, B; Chakraborty, P; Sundararaju, B or send Email.. Application In Synthesis of 3-Methylbenzoic acid

Application In Synthesis of 3-Methylbenzoic acid. In 2019 CHEMSUSCHEM published article about C-H ALKYLATION; N-ALKYLATION; SODIUM-BOROHYDRIDE; COOPERATIVE CATALYSIS; SECONDARY-AMINES; AROMATIC-AMINES; BRONSTED ACID; HYDROGENATION; AMINATION; MILD in [Emayavaramban, Balakumar; Chakraborty, Priyanka; Sundararaju, Basker] Indian Inst Technol Kanpur, Dept Chem, Kanpur 208016, Uttar Pradesh, India in 2019, Cited 78. The Name is 3-Methylbenzoic acid. Through research, I have a further understanding and discovery of 99-04-7.

Direct reductive alkylation of amines with carboxylic acid is carried out by using an inexpensive, air-stable cobalt/triphos catalytic system with molecular hydrogen as the reductant. This efficient synthetic method proceeds through reduction and condensation, followed by reduction of the in situ-generated imine into the amine in a green catalytic process.

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An article Development of Nickel-Based Negative Tone Metal Oxide Cluster Resists for Sub-10 nm Electron Beam and Helium Ion Beam Lithography WOS:000529924800041 published article about NANOPARTICLE PHOTORESISTS; ORGANIC FRAMEWORK; DESIGN in [Kumar, Rudra; Chauhan, Manvendra; Moinuddin, Mohamad G.; Sharma, Satinder K.] Indian Inst Technol IIT Mandi, Sch Comp & Elect Engn SCEE, Mandi 175005, Himachal Prades, India; [Gonsalves, Kenneth E.] Indian Inst Technol IIT Mandi, Sch Basic Sci SBS, Mandi 175005, Himachal Prades, India in 2020.0, Cited 61.0. Recommanded Product: 3-Methylbenzoic acid. The Name is 3-Methylbenzoic acid. Through research, I have a further understanding and discovery of 99-04-7

Hybrid metal-organic cluster resist materials, also termed as organo-inorganics, demonstrate their potential for use in next-generation lithography owing to their ability for patterning down to similar to 10 nm or below. High-resolution resist patterning is integrally associated with the compatibility of the resist and irradiation of the exposure source. Helium ion beam lithography (HIBL) is an emerging approach for the realization of sub-10 nm patterns at considerably lower line edge/width roughness (LER/LWR) and higher sensitivity as compared to electron beam lithography (EBL). Here, for the first time, a negative tone resist incorporating nickel (NO-based metal-organic clusters (Ni-MOCs) was synthesized and patterned using HIBL and EBL at 30 keV. This resist comprises a nickel-based metal building unit covalently linked with the organic ligand: m-toluic acid (C8H8O2). Dynamic light scattering confirmed a narrow size distribution of similar to 2 nm for metal-organic cluster (MOC) formulations. High-resolution similar to 9 nm HIBL line patterns were well developed at a sensitivity of 22 mu C/cm(2) and at a significantly low LER and LWR of 1.81 +/- 0.06 and 2.90 +/- 0.06 nm, respectively. Analogous high-resolution patterns were also observed in EBL with a sensitivity of 473 mu C/cm(2). Hence, the Ni-MOC-based resist investigated using HIBL and EBL elucidates the ability of its potential for the sub-10 nm technology node, under standard processing conditions.

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Safety of 3-Methylbenzoic acid. In 2019 ORG LETT published article about CATALYZED INTRAMOLECULAR HYDROAMINATION; PATHWAY DEPENDENT MALIGNANCIES; POTENT SMOOTHENED ANTAGONIST; FUSED PIPERAZINE; INTERMOLECULAR HYDROAMINATION; NEUROKININ-3 RECEPTOR; UNACTIVATED ALKENES; RAPID ACCESS; DERIVATIVES; ALKYNES in [Yamamoto, Koki; Inuki, Shinsuke; Ohno, Hiroaki; Oishi, Shinya] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan; [Yoshikawa, Yasushi; Ohue, Masahito] Tokyo Inst Technol, Sch Comp, Dept Comp Sci, Meguro Ku, Tokyo 1528550, Japan in 2019, Cited 58. The Name is 3-Methylbenzoic acid. Through research, I have a further understanding and discovery of 99-04-7.

An efficient method for the synthesis of [1,2,4]triazolo-[4,3-a]piperazine derivatives was established based on a gold(I)-catalyzed domino cyclization of an amidrazone substrate with a terminal alkyne. The amidoxime congeners were converted into [1,2,4]oxadiazolo[4,5-a]piperazine derivatives in the presence of a gold catalyst. The oxadiazolopiperazine is a promising scaffold for the design of novel inhibitors against p38 mitogen activated protein kinase (MAP kinase).

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Application In Synthesis of 3-Methylbenzoic acid. Authors Xu, KQ; Liu, L; Li, ZH; Huang, TZ; Xiang, K; Chen, TQ in AMER CHEMICAL SOC published article about in [Xu, Kaiqiang; Liu, Long; Li, Zhaohui; Huang, Tianzeng; Xiang, Kang; Chen, Tieqiao] Hainan Univ, Hainan Prov Fine Chem Engn Res Ctr, Hainan Prov Key Lab Fine Chem, Key Lab,Minist Educ Adv Mat Trop Isl Resources, Haikou 570228, Hainan, Peoples R China in 2020, Cited 64. The Name is 3-Methylbenzoic acid. Through research, I have a further understanding and discovery of 99-04-7

The controllable phosphorylations of thioesters were developed. When the reaction was catalyzed by a palladium catalyst, aryl or alkenyl phosphoryl compounds were generated through decarbonylative coupling, while the benzyl phosphoryl compounds were produced through deoxygenative coupling when the reaction was carried out in the presence of only a base.

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Quality Control of 3-Methylbenzoic acid. In 2019.0 J ORG CHEM published article about ALLYLIC SUBSTITUTION-REACTIONS; INTERMOLECULAR HYDROALKOXYLATION; HYDROAMINATION; PRONUCLEOPHILES; CONSTRUCTION; MECHANISM; TERTIARY; ESTERS in [Blieck, Remi; Taillefer, Marc; Monnier, Florian] CNRS, UMR 5253, Ecole Natl Super Chim Montpellier, Inst Charles Gerhardt Montpellier,AM2N, 8 Rue Ecole Normale, F-34296 Montpellier 5, France; [Monnier, Florian] IUF, 1 Rue Descartes, F-75231 Paris 5, France in 2019.0, Cited 42.0. The Name is 3-Methylbenzoic acid. Through research, I have a further understanding and discovery of 99-04-7.

The addition of carboxylic acids to allenes was performed with copper catalysis. This hydrocarboxylation reaction, occurring on the terminal carbon of the allenes, is totally regio- and stereoselective. It represents the first coppercatalyzed example of intermolecular C-O bond formation by allene hydrofunctionalization. This ligand-free system is based on the use of catalytic amounts of copper combined with a base (10 mol % of K2CO3).

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