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21677-57-6

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21677-57-6 Usage

Chemical class

Nitroimidazole derivative

Structure

Fused imidazole ring with a nitro group and an amine group at different positions

Applications

Medicinal chemistry

Properties

Antimicrobial and antiparasitic

Usage

Development of pharmaceutical drugs

Infections treated

Protozoal and bacterial infections

Potential use

Cancer therapy (selectively targets hypoxic tumor cells)

Field of importance

Medicine

Check Digit Verification of cas no

The CAS Registry Mumber 21677-57-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,7 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 21677-57:
(7*2)+(6*1)+(5*6)+(4*7)+(3*7)+(2*5)+(1*7)=116
116 % 10 = 6
So 21677-57-6 is a valid CAS Registry Number.

21677-57-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dimethyl-5-nitroimidazol-4-amine

1.2 Other means of identification

Product number -
Other names 5-amino-1,2-dimethyl-4-nitroimidazole

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:21677-57-6 SDS

21677-57-6Downstream Products

21677-57-6Relevant articles and documents

Transformations of the imidazole ring in 1-alkyl- and 1-aryl-4-nitroimidazoles following the attack of hydroxylamine or 4-amino-1,2,4-triazole

Suwinski, Jerzy,Swierczek, Krzysztof

, p. 1040 - 1046 (2007/10/03)

Novel imidazole-oxadiazole ring interconversions (transformations) accompanying nucleophilic amination of 4-nitroimidazoles by hydroxylamine or 4-amino-1,2,4-triazole are described with suggestions concerning mechanisms of the reactions. 1996 Plenum Publishing Corporation.

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