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85012-71-1

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85012-71-1 Usage

Structure

1H-Imidazole core with a methanol group (-OH) attached to the 5-position and a methyl group (-CH3) and a nitro group (-NO2) attached to the 1-position

Derivative of imidazole

Yes

Contains a nitro group

Yes

Classification

Nitroimidazole compound

Known for antimicrobial properties

Yes

Potential applications

Pharmaceutical industry (antimicrobial and antiparasitic drugs), research and development in medicine and biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 85012-71-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,1 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 85012-71:
(7*8)+(6*5)+(5*0)+(4*1)+(3*2)+(2*7)+(1*1)=111
111 % 10 = 1
So 85012-71-1 is a valid CAS Registry Number.

85012-71-1SDS

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 5-hydroxymethyl-1-methyl-4-nitro-1H-imidazole

1.2 Other means of identification

Product number -
Other names (1-methyl-4-nitro-1H-imidazol-5-yl)methanol

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:85012-71-1 SDS

85012-71-1Downstream Products

85012-71-1Relevant articles and documents

Synthesis and Evaluation of Nitroheterocyclic Carbamate Prodrugs for Use with Nitroreductase-Mediated Gene-Directed Enzyme Prodrug Therapy

Hay, Michael P.,Anderson, Robert F.,Ferry, Dianne M.,Wilson, William R.,Denny, William A.

, p. 5533 - 5545 (2007/10/03)

A variety of nitroheterocyclic carbamate prodrugs of phenylenediamine mustard and 5-amino-1-(chloromethyl)-3-[(5,6,7-trimethoxyindol-2-yl)carbonyl]-1, 2-dihydro-3H-benz[e]indoline (aminoseco-CBI-TMI), covering a wide range of reduction potential, were pre

Synthesis and calcium channel antagonist activity of 1,4-dihydropyridine derivatives containing 4-nitroimidazolyl substituents

Shafiee, Abbas,Rastkary, Noushin,Jorjani, Masoumeh

, p. 537 - 542 (2007/10/03)

Alkyl, cycloalkyl and arylalkyl ester analogues of nifedipine (CAS 21829-25-4), in which the ortho-nitro phenyl group at position 4 is replaced by 1-methyl-4-nitro-5-imidazolyl substituent, were synthesized and evaluated as calcium channel antagonists usi

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