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881637-11-2

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881637-11-2 Usage

General Description

2-Aminooxazole-5-carboxylic acid is a chemical compound with a molecular formula C4H3N3O3. It is a heterocyclic organic compound and a derivative of oxazole. This chemical is primarily used in pharmaceutical research as a building block for the synthesis of various bioactive molecules and pharmaceutical drugs. It has been studied for its potential therapeutic applications as an anticancer agent, as well as for the treatment of various bacterial and fungal infections. Additionally, 2-Aminooxazole-5-carboxylic acid has been investigated for its antioxidant properties and its potential use in the development of new materials and coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 881637-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,6,3 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 881637-11:
(8*8)+(7*8)+(6*1)+(5*6)+(4*3)+(3*7)+(2*1)+(1*1)=192
192 % 10 = 2
So 881637-11-2 is a valid CAS Registry Number.

881637-11-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Aminooxazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-amino-1,3-oxazole-5-carboxylic 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:881637-11-2 SDS

881637-11-2Downstream Products

881637-11-2Relevant articles and documents

Design, synthesis, and antibacterial properties of dual-ligand inhibitors of acetyl-CoA carboxylase

Silvers, Molly A.,Robertson, Gregory T.,Taylor, Carol M.,Waldrop, Grover L.

, p. 8947 - 8959 (2015/03/14)

There is an urgent demand for the development of new antibiotics due to the increase in drug-resistant pathogenic bacteria. A novel target is the multifunctional enzyme acetyl-CoA carboxylase (ACC), which catalyzes the first committed step in fatty acid s

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