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175424-74-5

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175424-74-5 Usage

General Description

N-[(6-chloro-3-pyridinyl)methyl]acetamide is a chemical compound with the formula C9H10ClN3O. It is an acetamide derivative with a chlorine-substituted pyridine ring and a methyl group attached to the amide nitrogen. N-[(6-chloro-3-pyridinyl)methyl]acetamide(SALTDATA: FREE) is widely used in the pharmaceutical industry as a building block in the synthesis of various drugs and biologically active molecules. It also exhibits a range of biological activities, including antimicrobial, antifungal, and anticancer properties, making it an important molecule for drug development and medicinal chemistry research. Additionally, this compound has been extensively studied for its potential use in agricultural pesticides and crop protection.

Check Digit Verification of cas no

The CAS Registry Mumber 175424-74-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,4,2 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 175424-74:
(8*1)+(7*7)+(6*5)+(5*4)+(4*2)+(3*4)+(2*7)+(1*4)=145
145 % 10 = 5
So 175424-74-5 is a valid CAS Registry Number.

175424-74-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(6-Chloropyridin-3-yl)methyl]acetamide

1.2 Other means of identification

Product number -
Other names 2-chloro-5-acetaminomethylpyridine

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:175424-74-5 SDS

175424-74-5Relevant articles and documents

Convenient synthesis of protected primary amines form nitriles

Caddick, Stephen,De K. Haynes, Alexandra K.,Judd, Duncan B.,Williams, Meredith R.V.

, p. 3513 - 3516 (2007/10/03)

Investigations into the use of nickel chloride and sodium borohydride for the reduction of nitriles showed the secondary amine dimers to be the major products under normal conditions. The addition of a suitable trapping agent, such as di-tert-butyl dicarbonate, allowed the isolation of the protected primary amines. (C) 2000 Elsevier Science Ltd.

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