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7372-07-8

7372-07-8

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7372-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7372-07-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,7 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7372-07:
(6*7)+(5*3)+(4*7)+(3*2)+(2*0)+(1*7)=98
98 % 10 = 8
So 7372-07-8 is a valid CAS Registry Number.

7372-07-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name LINOLELAIDOYL CHLORIDE

1.2 Other means of identification

Product number -
Other names octadeca-9,12-dienoyl chloride

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:7372-07-8 SDS

7372-07-8Upstream product

7372-07-8Downstream Products

7372-07-8Relevant articles and documents

Synthesis and antimycobacterial activity of isoniazid derivatives from renewable fatty acids

Rodrigues, Marieli O.,Cantos, Jéssica B.,D'Oca, Caroline R. Montes,Soares, Karina L.,Coelho, Tatiane S.,Piovesan, Luciana A.,Russowsky, Dennis,Da Silva, Pedro A.,D'Oca, Marcelo G. Montes

, p. 6910 - 6914 (2013/11/06)

This work describes the synthesis of a series of fatty acid hydrazide derivatives of isoniazid (INH). The compounds were tested against Mycobacterium tuberculosis H37Rv (ATCC 27294) as well as INH-resistant (ATCC 35822 and 1896 HF) and rifampicin-resistant (ATCC 35338) M. tuberculosis strains. The fatty acid derivatives of INH showed high antimycobacterial potency against the studied strains, which is desirable for a pharmaceutical compound, suggesting that the increased lipophilicity of isoniazid plays an important role in its antimycobacterial activity.

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