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146450-02-4

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146450-02-4 Usage

Structure

A five-membered heterocyclic ring compound containing nitrogen, with a carboxamide group and two methyl groups at positions 4 and 5 on the imidazole ring.

Type

A derivative of imidazole.

Possible applications

Pharmaceutical and biochemical.

Usage

May be used to influence various biological processes.

Research status

Further research and testing may be required to fully understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 146450-02-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,4,5 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 146450-02:
(8*1)+(7*4)+(6*6)+(5*4)+(4*5)+(3*0)+(2*0)+(1*2)=114
114 % 10 = 4
So 146450-02-4 is a valid CAS Registry Number.

146450-02-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Imidazole-2-carboxamide,4,5-dimethyl-(9CI)

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:146450-02-4 SDS

146450-02-4Downstream Products

146450-02-4Relevant articles and documents

A CONVENIENT AND NEW ONE-STEP SYNTHESIS OF 1H-IMIDAZOLE-2-CARBOXAMIDES

Singh, Baldev

, p. 2373 - 2378 (2007/10/02)

1,2-Diketone monophenylhydrazones (2) reacted with aminomalonamide in 1-methyl-2-pyrrolidinone to provide 1H-imidazole-2-carboxamides (4).The condensation of 1-(4-pyridinyl)-2-propanone with phenyldiazonium chloride gave 1-phenylhydrazono-1-(4-pyridinyl)-2-propanone (2a). 4-Methyl-5-(4-pyridinyl)-1H-imidazole-2-carboxamide (4a) was converted to the corresponding nitrile (5a) by the action of phosphorous oxychloride.

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