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343-73-7

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343-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 343-73-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 343-73:
(5*3)+(4*4)+(3*3)+(2*7)+(1*3)=57
57 % 10 = 7
So 343-73-7 is a valid CAS Registry Number.

343-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-Chloro-6-fluorophenyl)acetamide

1.2 Other means of identification

Product number -
Other names 4-Chlor-3-acetoxy-toluol

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:343-73-7 SDS

343-73-7Relevant articles and documents

BENZOTHIAZOLE COMPOUNDS AND USES THEREOF

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Paragraph 0398-0399, (2020/02/27)

Disclosed are compounds of Formula (I), methods of using the compounds for inhibiting HPK1 activity and pharmaceutical compositions comprising such compounds. The compounds are useful in treating, preventing or ameliorating diseases or disorders associate

Cobalt(II)-catalyzed regioselective C-H halogenation of anilides

Li, Ze-lin,Sun, Kang-kang,Cai, Chun

supporting information, p. 5433 - 5440 (2018/08/12)

A cobalt-catalyzed regioselective C-H halogenation methodology is reported herein. The highlight of this work is the highly selective C-H functionalization of anilides, which results in high-yielding, versatile, and practical halogenated products. Thereby, brominations, chlorinations and iodinations of many electron-rich and electron-deficient anilides were achieved in a highly selective fashion. Mechanistic studies with respect to the pathway of the reaction are also described.

Monoprotected l-Amino Acid (l-MPAA), Accelerated Bromination, Chlorination, and Iodination of C(sp2)?H Bonds by Iridium(III) Catalysis

Kathiravan, Subban,Nicholls, Ian A.

supporting information, p. 7031 - 7036 (2017/05/29)

Halogenated arenes are important structural motifs commonly found in biologically active molecules and used for a variety of transformations in organic synthesis. Herein, we report the mono-protected l-amino acid (l-MPAA) accelerated iridium(III)-catalyzed halogenation of (hetero)anilides at room temperature. This reaction constitutes the first example of an iridium(III)/l-MPAA-catalyzed general halogenation of (hetero)arenes through C(sp2)?H activation. Furthermore, we demonstrate the potential utility of our method through its use in the synthesis of a quinolone derivative.

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