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56894-29-2

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56894-29-2 Usage

Chemical structure

1H-imidazole derivative with a 3-chloropropyl group and a 5-nitro-2-methyl group

Industry use

Pharmaceutical industry

Properties

Antibacterial, antifungal, anti-inflammatory, and analgesic

Applications

a. Active ingredient in pharmaceuticals
b. Chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals

Potential

Candidate for the development of new drugs due to its multiple properties

Check Digit Verification of cas no

The CAS Registry Mumber 56894-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,9 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56894-29:
(7*5)+(6*6)+(5*8)+(4*9)+(3*4)+(2*2)+(1*9)=172
172 % 10 = 2
So 56894-29-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H10ClN3O2/c1-6-9-5-7(11(12)13)10(6)4-2-3-8/h5H,2-4H2,1H3

56894-29-2SDS

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 1-(3-chloropropyl)-2-methyl-5-nitroimidazole

1.2 Other means of identification

Product number -
Other names EINECS 260-421-2

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:56894-29-2 SDS

56894-29-2Relevant articles and documents

Synthesis and prediction of bioactivity of new nitroimidazole derivatives

Kowalski, Piotr,Nowak, Krystyna,Szpakiewicz, Barbara

, p. 883 - 888 (2005)

Syntheses of 1-propyl derivatives of 2-methyl-5-nitroimidazole (11-17), containing various azanaphthalene systems attached at 3-position of the propyl group have been described. Due to structural similarity of the derivatives 11-17 with metronidazole, an

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