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38132-38-6

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38132-38-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38132-38-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,3 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 38132-38:
(7*3)+(6*8)+(5*1)+(4*3)+(3*2)+(2*3)+(1*8)=106
106 % 10 = 6
So 38132-38-6 is a valid CAS Registry Number.

38132-38-6SDS

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 benzoylformic acid semicarbazone

1.2 Other means of identification

Product number -
Other names Phenylglyoxylsaeure-semicarbazon

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:38132-38-6 SDS

38132-38-6Relevant articles and documents

Synthesis and antimicrobial evaluation of 6-azauracil non-nucleosides

El-Brollosy, Nasser R.

scheme or table, p. 1483 - 1490 (2009/12/26)

The present study describes synthesis and antimicrobial evaluation of a series of novel 6-azauracil non-nucleosides. Reaction of silylated 6-azauracils with the appropriate chloroethers gave the corresponding non-nucleosides. 1-(Allyloxymethy)-6-azauracils and non-nucleosides bearing indanyl, cyclohexenyl, and cyclohexyl moieties were obtained via silylation of 6-azauracils followed by treatment with the appropriate acetals. Selected compounds were tested for their in vitro antimicrobial activity against a panel of standard strains of Gram-positive and Gram-negative bacteria and the yeast-like pathogenic fungus Candida albicans. Four compounds showed marked inhibitory activity particularly against the tested Gram-positive bacteria.

Gonadotropin-releasing hormone receptor antagonists and methods relating thereto

-

, (2008/06/13)

GnRH receptor antagonists are disclosed which have utility in the treatment of a variety of sex-hormone related conditions in both men and women. The compounds of this invention have the structure: wherein R1, R2, R3a, Rs

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