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93270-70-3

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93270-70-3 Usage

Derivative of imidazole

The compound is based on the imidazole ring structure.

Carboxamide group

Contains a -CONH2 group, which may contribute to its potential pharmaceutical applications.

Amino group

Contains an -NH2 group, which can be important in the design of bioactive compounds.

4-Methoxyphenyl group

A methoxy (-OCH3) group attached to a phenyl ring, contributing to the compound's unique properties and functionality.

Potential pharmaceutical applications

Due to the presence of imidazole and amino groups, the compound may be useful in drug development and targeting various biological processes.

Need for further studies

To determine specific uses and potential effects of the compound.

Check Digit Verification of cas no

The CAS Registry Mumber 93270-70-3 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 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93270-70:
(7*9)+(6*3)+(5*2)+(4*7)+(3*0)+(2*7)+(1*0)=133
133 % 10 = 3
So 93270-70-3 is a valid CAS Registry Number.

93270-70-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-amino-1-(4-methoxyphenyl)imidazole-4-carboxamide

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:93270-70-3 SDS

93270-70-3Relevant articles and documents

A domino type one-flask synthesis of 1-substituted-5-aminoimidazole-4- carboxamides and ring transformation to pyrazine under microwave through suitable aminoimidazoliumcarboxamide

Chattopadhyay, Gautam,Saha, Tapas K.

, p. 827 - 830 (2007/10/03)

Reductive heterocyclisation of oximinocyanoacetamide 1 in the presence of ethyl orthoformate and appropriate amine affords 1-substituted-5-aminoimidazole- 4-carboxamides 2. 4-Amino-5-carboxamido-3-diphenylmethyl-1-phenacylimidazolium bromide 4c, generated

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