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1H-Imidazole-2-carboxylic acid, 4-(acetylamino)-1-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

225667-16-3

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225667-16-3 Usage

Structure

An imidazole ring with a carboxylic acid group at position 2, an acetylamino group at position 4, and a methyl group at position 1

Derivative of

Imidazole-2-carboxylic acid

Usage

Building block for the synthesis of pharmaceutical and agricultural compounds

Chelating agent

Can bind to metal ions, useful in chemical processes and applications

Therapeutic potential

Being investigated for potential use in the treatment of various medical conditions

Check Digit Verification of cas no

The CAS Registry Mumber 225667-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,6,6 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 225667-16:
(8*2)+(7*2)+(6*5)+(5*6)+(4*6)+(3*7)+(2*1)+(1*6)=143
143 % 10 = 3
So 225667-16-3 is a valid CAS Registry Number.

225667-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-acetamido-1-methylimidazole-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names -

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:225667-16-3 SDS

225667-16-3Downstream Products

225667-16-3Relevant articles and documents

Sequence-specific DNA alkylation by hybrid molecules between segment A of duocarmycin A and pyrrole/imidazole diamide

Tao, Zhi-Fu,Fujiwara, Tsuyoshi,Saito, Isao,Sugiyama, Hiroshi

, p. 650 - 653 (2007/10/03)

In the absence of distamycin A (Dist), hybrids 1 (X = N, CH) selectively alkylate the 3' end of adenine in AT-rich DNA sequences. However, these hybrids can form a heterodimer with Dist to alkylate G residues of predetermined DNA sequences efficiently and with high selectivity.

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