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18370-10-0

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18370-10-0 Usage

Chemical Properties

Off-white powder

Check Digit Verification of cas no

The CAS Registry Mumber 18370-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,7 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18370-10:
(7*1)+(6*8)+(5*3)+(4*7)+(3*0)+(2*1)+(1*0)=100
100 % 10 = 0
So 18370-10-0 is a valid CAS Registry Number.

18370-10-0 Well-known Company Product Price

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  • Alfa Aesar

  • (H56565)  3-Chloro-N-methylbenzamide, 97%   

  • 18370-10-0

  • 250mg

  • 1470.0CNY

  • Detail
  • Alfa Aesar

  • (H56565)  3-Chloro-N-methylbenzamide, 97%   

  • 18370-10-0

  • 1g

  • 4704.0CNY

  • Detail

18370-10-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-N-methylbenzamide

1.2 Other means of identification

Product number -
Other names 3-chloro-N-methyl-benzamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:18370-10-0 SDS

18370-10-0Relevant articles and documents

Palladium-Catalyzed Direct C-H Trifluoroethylation of Aromatic Amides

Maraswami, Manikantha,Pankajakshan, Sreekumar,Chen, Gang,Loh, Teck-Peng

, p. 4223 - 4226 (2017)

A simple and direct C-H trifluoroethylation of aromatic amides has been developed. The protocol is applicable to a variety of aromatic amides, including ones derived from amino acids. The developed method can be used for further modifications of peptides. Preliminary mechanistic studies have been done by isolating the reaction intermediate.

Catalytic asymmetric [3+2] cycloaddition of isomünchnones with methyleneindolinones

Feng, Xiaoming,Hu, Xinyue,Lin, Lili,Wang, Kaixuan,Xu, Chaoran,Zhou, Yuqiao

supporting information, p. 8917 - 8920 (2021/09/10)

An efficient enantioselective [3+2] cycloaddition of isomünchnones with methyleneindolinones that are generated by anin situintramolecular addition of the carbonyl group to rhodium carbenes is realized with a chiralN,N′-dioxide/Zn(ii) complex as a Lewis acid. A series of chiral oxa-bridged 3-spiropiperidines are obtained in high yields with excellent dr and excellent ee values.

Formation of Aryl [1-Cyano-4-(dialkylamino)butadienyl] Ketones from Pyridines

Gim, Hyo Jin,Jung, Michael E.

supporting information, p. 2548 - 2552 (2019/06/08)

Treatment of 2-chloropyridine with LDA and the Weinreb amide of benzoic acid afforded three unusual products, namely N -methylbenzamide, 2-chloropyridine-3-methanol, and the ring-opened addition product. This same final product could also be obtained from 2-chloro-3-benzoylpyridine on treatment with LDA. Mechanistic insight for the formation of these products is provided.

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