Chemical Research in 87-63-8

Application In Synthesis of 2-Chloro-6-methylaniline. About 2-Chloro-6-methylaniline, If you have any questions, you can contact Li, X; Xie, WJ; Wang, XT; Huang, ZZ; Bian, XL; Wang, KW; Sun, Q or concate me.

An article Chemical conversion of nicotinamide into type I positive allosteric modulator of alpha 7 nAChRs WOS:000471750200013 published article about ACETYLCHOLINE-RECEPTOR AGONIST; PHARMACOLOGICAL CHARACTERIZATION; IDENTIFICATION; APOPTOSIS; SUBUNIT; RELEASE in [Li, Xin; Xie, Wenjun; Huang, Zongze; Sun, Qi] Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China; [Xie, Wenjun; Wang, Xintong; Bian, Xiling; Wang, KeWei] Peking Univ, Sch Pharmaceut Sci, Dept Mol & Cellular Pharmacol, Beijing 100191, Peoples R China; [Wang, KeWei] Qingdao Univ, Sch Pharm, Dept Pharmacol, Qingdao 266021, Shandong, Peoples R China in 2019, Cited 38. The Name is 2-Chloro-6-methylaniline. Through research, I have a further understanding and discovery of 87-63-8. Application In Synthesis of 2-Chloro-6-methylaniline

Structural modifications of nicotinamide, a form of vitamin B3, gave rise to a series of compounds (8aa-8ce) that exhibit activities as type I positive allosteric modulators (PAMs) of human alpha 7 nAChR expressed in Xenopus oocytes in two-electrode voltage clamp assay. The compound 8ai was a potent and efficacious PAM with an EC50 = 3.34 +/- 1.13 mu M and the maximum activation effect of alpha 7 current over 1474 +/- 246% in the presence of acetylcholine (100 mu M). It is highly specific to alpha 7 nAChR over other subtypes of nAChR and 5-HT3A receptors. The structure-activity relationship analysis identified a key skeleton of nicotinamide nucleus critical for biological activity. Taken together, the 8ai as a type I PAM of alpha 7 nAChR may be beneficial for improvement of cognitive deficit.

Application In Synthesis of 2-Chloro-6-methylaniline. About 2-Chloro-6-methylaniline, If you have any questions, you can contact Li, X; Xie, WJ; Wang, XT; Huang, ZZ; Bian, XL; Wang, KW; Sun, Q or concate me.

Reference:
Patent; ASTRAZENECA AB; NPS PHARMACEUTICALS, INC.; WO2006/20879; (2006); A1;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Extracurricular laboratory: Synthetic route of C7H7Cl

Safety of 1-Chloro-2-methylbenzene. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Sarmah, K; Mukhopadhyay, S; Maji, TK; Pratihar, S or concate me.

An article Switchable Bifunctional Bistate Reusable ZnO-Cu for Selective Oxidation and Reduction Reaction WOS:000455286600075 published article about RING-OPENING POLYMERIZATION; PHOTOSWITCHABLE CATALYSIS; TRANSFER HYDROGENATION; LEWIS-ACID; LIGHT; COMPLEX; RUTHENIUM; CHEMISTRY; COPOLYMERIZATION; NANOPARTICLES in [Sarmah, Kasturi; Mukhopadhyay, Subhamoy; Maji, Tarun K.; Pratihar, Sanjay] Tezpur Univ, Dept Chem Sci, Napaam 784028, Assam, India in 2019.0, Cited 75.0. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8. Safety of 1-Chloro-2-methylbenzene

Herein we disclosed the utilization of copper loaded zinc oxide (ZnO-Cu) for its stimuli (O-2/light) responsive switchable performance between its reduced (S-1) and oxidized (S-2) state for two antagonistic reactions, namely oxidation of alkyl arenes/heteroarenes to aldehydes/ketones and reduction of nitro arenes/heteroarenes corresponding amines. The two states of the catalyst showed its switchable performance as highly active and poorly active catalyst for oxidation and reduction, and both reactions could be turned off and on by changing the stimuli (light and O-2/N-2). The switching efficiency between the states and their relative reactivity were found to be consistent under variety of reaction conditions and remain unaltered irrespective of oxidation-reduction (or vice versa) sequence and substrates used in the reaction. The photo catalysts (S-1 and S-2) demonstrated good catalytic activity, multiple reusability, broad substrate scope, and reasonable functional group tolerance for both the reactions and probed its quality performance in a large-scale setup. The system was used in an assisted tandem catalysis setup for the synthesis of benzyl amines utilizing both oxidation and reduction reaction by stimuli responsive switching between the states of the catalyst.

Safety of 1-Chloro-2-methylbenzene. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Sarmah, K; Mukhopadhyay, S; Maji, TK; Pratihar, S or concate me.

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

An update on the compound challenge: 95-49-8

About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Ray, R; Hartwig, JF or concate me.. Recommanded Product: 95-49-8

Authors Ray, R; Hartwig, JF in WILEY-V C H VERLAG GMBH published article about in [Ray, Ritwika; Hartwig, John F.] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA in 2021.0, Cited 67.0. Recommanded Product: 95-49-8. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8

Here, we report a class of ligands based on oxalohydrazide cores and N-amino pyrrole and N-amino indole units that generates long-lived copper catalysts for couplings that form the C-O bonds in biaryl ethers. These Cu-catalyzed coupling of phenols with aryl bromides occurred with turnovers up to 8000, a value which is nearly two orders of magnitude higher than those of prior couplings to form biaryl ethers and nearly an order of magnitude higher than those of any prior copper-catalyzed coupling of aryl bromides and chlorides. This ligand also led to copper systems that catalyze the coupling of aryl chlorides with phenols and the coupling of aryl bromides and iodides with primary benzylic and aliphatic alcohols. A wide variety of functional groups including nitriles, halides, ethers, ketones, amines, esters, amides, vinylarenes, alcohols and boronic acid esters were tolerated, and reactions occurred with aryl bromides in pharmaceutically related structures.

About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Ray, R; Hartwig, JF or concate me.. Recommanded Product: 95-49-8

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

The Best Chemistry compound:C7H4Cl2O2

About 2,6-Dichlorobenzoic acid, If you have any questions, you can contact Dong, LL; Shen, SQ; Chen, W; Lu, HZ; Xu, DD; Jin, SH; Yang, Q; Zhang, JJ or concate me.. Quality Control of 2,6-Dichlorobenzoic acid

I found the field of Biochemistry & Molecular Biology; Pharmacology & Pharmacy; Chemistry very interesting. Saw the article Glycosyl triazoles as novel insect beta-N-acetylhexosaminidase OfHex1 inhibitors: Design, synthesis, molecular docking and MD simulations published in 2019.0. Quality Control of 2,6-Dichlorobenzoic acid, Reprint Addresses Zhang, JJ (corresponding author), China Agr Univ, Coll Sci, Dept Appl Chem, Beijing, Peoples R China.; Yang, Q (corresponding author), Dalian Univ Technol, Sch Life Sci & Biotechnol, Dalian, Peoples R China.; Yang, Q (corresponding author), Chinese Acad Agr Sci, Inst Plant Protect, Beijing 100193, Peoples R China.. The CAS is 50-30-6. Through research, I have a further understanding and discovery of 2,6-Dichlorobenzoic acid

The insect enzyme GH20 beta-N-acetyl-D-hexosaminidase OfHex1 represents an important chitinolytic enzyme found in the agricultural pest Ostrinia furnacalis (Guenee) and inhibition of this enzyme has been considered a promising strategy for the development of eco-friendly pesticides. In this article, based on the structure of the catalytic domains of OfHex1, a series of novel glycosyl triazoles were designed and synthesized via Cu-catalyzed azide-alkyne [3+ 2] cycloaddition reaction. To investigate the potency and selectivity of these glycosyl triazoles, the inhibition activities towards OfHex1 and HsHexB (human beta-N-acetylhexosaminidase B) were studied. Particularly compound 17c (OfHex1, K-i= 28.68 mu M; HsHexB, K-i > 100 mu M) exhibited a suitable activity and selectivity against OfHex1. Furthermore, the possible inhibitory mechanisms of 17c with OfHex1 were studied using molecular docking and MD simulations. The structure-activity relationship results as well as the formed binding patterns may provide promising insights into the further development of novel OfHex1 inhibitors.

About 2,6-Dichlorobenzoic acid, If you have any questions, you can contact Dong, LL; Shen, SQ; Chen, W; Lu, HZ; Xu, DD; Jin, SH; Yang, Q; Zhang, JJ or concate me.. Quality Control of 2,6-Dichlorobenzoic acid

Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics

Why do aromatic interactions matter of compound:C7H7Cl

Computed Properties of C7H7Cl. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Liao, RQ; Li, WT; Kang, ZJ; Tang, L; Yang, B; Wang, L or concate me.

In 2019.0 ENVIRON MONIT ASSESS published article about POLYCHLORINATED-BIPHENYLS PCBS; POLYBROMINATED DIPHENYL ETHERS; AROMATIC-HYDROCARBONS PAHS; DIBENZO-P-DIOXINS; SPATIAL-DISTRIBUTION; MARINE FISH; ESTUARY; TRENDS; PBDES; WATER in [Liao, Riquan; Kang, Zhenjun; Yang, Bin] Beibu Gulf Univ, Guangxi Key Lab Beibu Gulf Marine Biodivers Conse, Qinzhou 535000, Guangxi, Peoples R China; [Li, Weitao; Wang, Liang] Shanghai Univ, Inst Nanochem & Nanobiol, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China; [Tang, Liang] Shanghai Univ, Shanghai Inst Appl Radiat, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China in 2019.0, Cited 28.0. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8. Computed Properties of C7H7Cl

To enhance our understanding on environmental conditions of the Maowei Sea in Guangxi province, China, the concentration and distribution of 22 chlorobenzene compounds (CBs) in the surface sediment were determined by gas chromatography-mass spectrometry (GC-MS). The relationship of the sediment between CBs and total organic carbon (TOC) was also investigated. The results showed that a total of eight kinds of CBs compounds were detected in the sediment samples which were collected from the coastal environment of the Maowei Sea, with an average concentration of 15.3ngg(-1) (the concentration range, 2.5-61.5ngg(-1)). The rank of their average concentrations was as follows: 2,3,4,5,6-pentachlorotoluene>hexachlorobenzene, 2-chlorotoluene, 3-chlorotoluene and 2,3-dichlorotoluene>2,4-dichlorotoluene>4-chlorotoluene>pentachlorobenzene. Most CBs were distributed in sediments along the east coast of the Maowei Sea. For total TOC content in sediments, the concentration in the sampling locations was similar, with a mean concentration of 8.83gkg(-1) (the concentration range, 4.87-20.13gkg(-1)). However, there was no significant correlation between the concentration of TOC and total CBs. Compared to the corresponding CBs in the sediment of other coastal areas in mainland China and other countries, the value of CBs in the Maowei Sea was low.

Computed Properties of C7H7Cl. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Liao, RQ; Li, WT; Kang, ZJ; Tang, L; Yang, B; Wang, L or concate me.

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Downstream Synthetic Route Of C7H7Cl

SDS of cas: 95-49-8. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Yang, F; Hu, HY; Gao, Q; Yang, YH; Tang, H; Xie, K; Liu, H; He, Y; Yao, H or concate me.

SDS of cas: 95-49-8. Yang, F; Hu, HY; Gao, Q; Yang, YH; Tang, H; Xie, K; Liu, H; He, Y; Yao, H in [Yang, Fu; Hu, Hongyun; Gao, Qiang; Yang, Yuhan; Tang, Hua; Xie, Kang; Liu, Huan; Yao, Hong] Huazhong Univ Sci & Technol, Sch Energy & Power Engn, State Key Lab Coal Combust, Wuhan 430074, Peoples R China; [Liu, Huan] Huazhong Univ Sci & Technol, Sch Energy & Power Engn, Dept New Energy Sci & Engn, Wuhan 430074, Peoples R China; [He, Yao] Guangdong Univ Technol, Sch Environm Sci & Engn, Inst Environm Hlth & Pollut Control, Guangzhou Key Lab Environm Catalysis & Pollut Con, Guangzhou 510006, Peoples R China published Study on the influence of small molecular gases on toluene reforming in molten salt in 2020.0, Cited 32.0. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8.

The upgrading of tar is a key issue for the sufficient application of biowaste pyrolysis technology. Molten salt, with high migration and diffusion of ions to prevent the deactivation of coke deposition of tar reforming functional metals, is considered as a feasible catalytic reaction medium and heat carrier for the upgrading of tar. The present study investigated the interactions between small molecular pyrolysis gases (including H-2, CO, CH4) and main tar model compound in ternary carbonate eutectics (Li2CO3-Na2CO3-K2CO3). The results demonstrated that H-2 could be decomposed to produce H radicals, promoting the conversion of toluene into gaseous products. CO32- could consume H radicals required by toluene cracking, making the process toluene polymerized to polycyclic aromatic hydrocarbons be strengthened. On the other hand, CO would react with OH radicals to produce H radicals and could enhance gas-generating process. In addition, toluene could react with CO to form benzaldehyde and phenylacetaldehyde. With the addition of CH4, more H radicals were supposed to be consumed, and toluene cracking process was further inhibited. Finally, the effect sequence of small molecular gases (H-2 > CH4 > CO) on toluene reforming reaction was authenticated by investigating the impacts of introducing any two gases in toluene reforming. (C) 2020 Elsevier Ltd. All rights reserved.

SDS of cas: 95-49-8. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Yang, F; Hu, HY; Gao, Q; Yang, YH; Tang, H; Xie, K; Liu, H; He, Y; Yao, H or concate me.

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Something interesting about 50-84-0

Recommanded Product: 50-84-0. About 2,4-Dichlorobenzoic acid, If you have any questions, you can contact Ma, YY; Shi, YQ; Yang, F; Wu, YS; Wu, YJ or concate me.

Ma, YY; Shi, YQ; Yang, F; Wu, YS; Wu, YJ in [Ma, Yueyue; Shi, Yaqi; Yang, Fan; Wu, Yangjie] Zhengzhou Univ, Key Lab Appl Chem Henan Univ, Henan Key Lab Chem Biol & Organ, Coll Chem & Mol Engn, Zhengzhou 450052, Henan, Peoples R China; [Wu, Yusheng] TetranovBiophann LLC, Zhengzhou 450001, Henan, Peoples R China; [Wu, Yusheng] Collaborat Innovat Ctr New Drug Res & Safety Eval, Zhengzhou 450001, Henan, Peoples R China published Merging photoredox catalysis with transition metal catalysis: Direct C4-H amination of 8-hydroxyquinoline derivatives in 2019, Cited 35. Recommanded Product: 50-84-0. The Name is 2,4-Dichlorobenzoic acid. Through research, I have a further understanding and discovery of 50-84-0.

A practical and efficient protocol for Ag/Ru-cocatalyzed regioselective C-H amination of 8-hydroxyquinoline esters with pyrazoles was developed, This reaction proceeded smoothly via a photoredox-mediated direct C-H/N-H oxidative coupling process. The remarkable features of this reaction include the wide substrate scope, mild reaction conditions and high regioselectivity at the C4 site of the quinolinyl moiety. (C) 2019 Elsevier Ltd. All rights reserved.

Recommanded Product: 50-84-0. About 2,4-Dichlorobenzoic acid, If you have any questions, you can contact Ma, YY; Shi, YQ; Yang, F; Wu, YS; Wu, YJ or concate me.

Reference:
Chloride – Wikipedia,
,Chlorides – an overview | ScienceDirect Topics

Interesting scientific research on C7H7Cl

About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Shen, HM; Qi, B; Hu, MY; Liu, L; Ye, HL; She, YB or concate me.. COA of Formula: C7H7Cl

An article Selective Solvent-Free and Additive-Free Oxidation of Primary Benzylic C-H Bonds with O-2 Catalyzed by the Combination of Metalloporphyrin with N-Hydroxyphthalimide WOS:000558395000001 published article about METAL-ORGANIC FRAMEWORKS; AEROBIC OXIDATION; CYCLOHEXANE OXIDATION; GREEN CHEMISTRY; TOLUENE; EFFICIENT; PERFORMANCE; PORPHYRINS; MANGANESE; COMPLEX in [Shen, Hai-Min; Qi, Bei; Hu, Meng-Yun; Liu, Lei; Ye, Hong-Liang; She, Yuan-Bin] Zhejiang Univ Technol, Coll Chem Engn, State Key Lab Breeding Base Green Chem Synth Tech, Hangzhou 310014, Peoples R China in 2020, Cited 75. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8. COA of Formula: C7H7Cl

A protocol for solvent-free and additive-free oxidation of primary benzylic C-H bonds with O(2)was presented through adjusting the combination of metalloporphyrins and NHPI as binary catalysts to overcome the deficiencies encountered in current oxidation systems. The effects of reaction temperature, porphyrin structure, central metal, catalyst loading and O(2)pressure were investigated systematically. For the optimized combination of T(2-OCH3)PPCo and NHPI, all the primary benzylic C-H bonds could be functionalized efficiently and selectively at 120 degrees C and 1.0 MPa O(2)with aromatic acids as the primary products. The selectivity towards aromatic acids could reach up to 70-95% in the conversion of more than 30% for most of the substrates possessing primary benzylic C-H bonds in the metalloporphyrin loading of 0.012% (mol/mol). And the superior performance of T(2-OCH3)PPCo among the metalloporphyrins investigated was mainly attributed to its high efficiency in charge transfer and fewer positive charges around central metal Co (II) which favored the adduction of O-2 to cobalt (II) forming the high-valence metal-oxo complex followed by the production of phthalimide N-oxyl radical (PINO) and the initiation of the catalytic oxidation cycle. This work would provide not only an efficient protocol in utilization of hydrocarbons containing primary benzylic C-H bonds, but also a significant reference in the construction of more efficient C-H bonds oxidation systems Graphic Abstract The solvent-free and additive-free oxidation of primary benzylic C-H bonds with O(2)was presented through adjusting the combination of metalloporphyrins and NHPI as binary catalysts, and the highest selectivity towards aromatic acid reached up to 95.1% with the conversion of 88.5% in the optimized combination of T(2-OCH3)PPCo and NHPI. [GRAPHICS] .

About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Shen, HM; Qi, B; Hu, MY; Liu, L; Ye, HL; She, YB or concate me.. COA of Formula: C7H7Cl

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

What advice would you give a new faculty member or graduate student interested in a career 95-49-8

Name: 1-Chloro-2-methylbenzene. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Li, JP; Huang, CY; Wen, DH; Zheng, QS; Tu, B; Tu, T or concate me.

Name: 1-Chloro-2-methylbenzene. Authors Li, JP; Huang, CY; Wen, DH; Zheng, QS; Tu, B; Tu, T in AMER CHEMICAL SOC published article about in [Li, Jinpeng; Huang, Changyu; Wen, Daheng; Zheng, Qingshu; Tu, Bo; Tu, Tao] Fudan Univ, Dept Chem, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200438, Peoples R China; [Tu, Tao] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China; [Tu, Tao] Zhengzhou Univ, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China; [Tu, Tao] Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R China in 2021, Cited 33. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8

A nickel-catalyzed amination of aryl chlorides with diverse amides via C-N bond cleavage has been realized under mild conditions. A broad substrate scope with excellent functional group tolerance at a low catalyst loading makes the protocol powerful for synthesizing various aromatic amines. The aryl chlorides could selectively couple to the amino fragments rather than the carbonyl moieties of amides. Our protocol complements the conventional amination of aryl chlorides and expands the usage of inactive amides.

Name: 1-Chloro-2-methylbenzene. About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Li, JP; Huang, CY; Wen, DH; Zheng, QS; Tu, B; Tu, T or concate me.

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Interesting scientific research on 95-49-8

About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Beutner, GL; Coombs, JR; Green, RA; Inankur, B; Lin, D; Qiu, J; Roberts, F; Simmons, EM; Wisniewski, SR or concate me.. HPLC of Formula: C7H7Cl

HPLC of Formula: C7H7Cl. In 2019.0 ORG PROCESS RES DEV published article about CROSS-COUPLING REACTIONS; FUNCTIONAL-GROUP COMPATIBILITY; LARGE-SCALE SYNTHESIS; LONG-LIVED CATALYSTS; ONE-POT SYNTHESIS; C-N; OXIDATIVE ADDITION; ALPHA-CARBOLINES; ARYL AMINATION; SCOPE in [Beutner, Gregory L.; Coombs, John R.; Green, Rebecca A.; Inankur, Bahar; Lin, Dong; Qiu, Jun; Roberts, Frederick; Simmons, Eric M.; Wisniewski, Steven R.] Bristol Myers Squibb Co, Chem & Synthet Dev, One Squibb Dr, New Brunswick, NJ 08903 USA in 2019.0, Cited 69.0. The Name is 1-Chloro-2-methylbenzene. Through research, I have a further understanding and discovery of 95-49-8.

The palladium-catalyzed coupling of aryl and heteroaryl chlorides with primary amides under mild homogeneous reaction conditions is reported. Successful C-N coupling is enabled by the use of a unique dual-base system consisting of DBU and NaTFA, which serve as proton acceptor and halide scavenger, respectively, using low catalyst loadings (0.5 mol %) with readily available, air-stable palladium precatalysts. The DBU/NaTFA system also enables the room-temperature coupling of primary aryl amines with aryl chlorides and is tolerant of a variety of base-sensitive functional groups.

About 1-Chloro-2-methylbenzene, If you have any questions, you can contact Beutner, GL; Coombs, JR; Green, RA; Inankur, B; Lin, D; Qiu, J; Roberts, F; Simmons, EM; Wisniewski, SR or concate me.. HPLC of Formula: C7H7Cl

Reference:
Patent; Nanjing Zhongteng Chemical Co., Ltd.; Zhong Hua; Lu Minshan; Chen Xiuzhen; Liu Qiaobao; Yin Hengbo; Wang Aili; (8 pag.)CN104876790; (2017); B;,
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics