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1000576-38-4

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1000576-38-4 Usage

General Description

Methyl 2-aminooxazole-4-carboxylate is a chemical compound with the molecular formula C5H6N2O3. It is a derivative of 2-aminooxazole-4-carboxylic acid and is commonly used in the synthesis of various pharmaceuticals and agrochemicals. Methyl 2-aminooxazole-4-carboxylate is a white to light yellow solid with a faint odor, and it is soluble in water and organic solvents. Methyl 2-aminooxazole-4-carboxylate has potential applications in the pharmaceutical industry, particularly in the development of new drugs and medications due to its unique chemical structure and properties. However, it should be handled and used with caution, following proper safety protocols and guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 1000576-38-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,5,7 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1000576-38:
(9*1)+(8*0)+(7*0)+(6*0)+(5*5)+(4*7)+(3*6)+(2*3)+(1*8)=94
94 % 10 = 4
So 1000576-38-4 is a valid CAS Registry Number.

1000576-38-4SDS

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 Methyl 2-aminooxazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 2-amino-1,3-oxazole-4-carboxylate

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:1000576-38-4 SDS

1000576-38-4Relevant articles and documents

Phenyl-oxazoles, a new family of inverse agonists at the H3 histamine receptor

Denonne, Frederic,Atienzar, Franck,Celanire, Sylvain,Christophe, Bernard,Delannois, Frederique,Delaunoy, Christel,Delporte, Marie-Laure,Durieu, Vronique,Gillard, Michel,Lallemand, Bndicte,Lamberty, Yves,Lorent, Genevive,Vanbellinghen, Alain,Van Houtvin, Nathalie,Verbois, Valrie,Provins, Laurent

scheme or table, p. 206 - 212 (2010/12/24)

(Chemical Equation Presented) Drug design: Oxazoles and thiazoles were designed and synthesised based on previously reported ligands of the 3rd histamine receptor (H3R). The aminopropoxy-phenyl-oxazole chemotype was identified as a promising H

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