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93276-75-6

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93276-75-6 Usage

Chemical Class

Isoxazole derivatives

Functional Groups

Cyano and methyl group

Uses

Synthesis of pharmaceuticals and agrochemicals

Potential Applications

Medicinal chemistry and drug development

Research Needs

Further research required to understand its potential uses and effects

Check Digit Verification of cas no

The CAS Registry Mumber 93276-75-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,7 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93276-75:
(7*9)+(6*3)+(5*2)+(4*7)+(3*6)+(2*7)+(1*5)=156
156 % 10 = 6
So 93276-75-6 is a valid CAS Registry Number.

93276-75-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-Cyano-5-methylisoxazol-3-yl)acetic acid

1.2 Other means of identification

Product number -
Other names (4-Cyano-5-methyl-isoxazol-3-yl)-acetic acid

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:93276-75-6 SDS

93276-75-6Relevant articles and documents

Isoxazole-Oxazole Conversion by Beckmann Rearrangement

Doleschall, Gabor,Seres, Peter

, p. 1875 - 1880 (2007/10/02)

A novel base-catalysed isoxazole-oxazole ring transformation was realized in the conversion of ethyl 5-hydroxy-3-(5-methylisoxazol-4-yl)isoxazole-4-carboxylate into 4-cyano-5-methyloxazol-2-ylacetic acid.A new process was developed for the preparation of t-4-amino-c-2-methyl-6-oxotetrahydropyran-r-3-carboxylic acid hydrochloride, a starting material for the synthesis of thienamycin.

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