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54255-79-7

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54255-79-7 Usage

Structure

Benzimidazole derivative with a chlorine atom and a nitro group attached to the phenyl ring

Usage

Pharmaceutical and agrochemical applications, building block in the synthesis of biologically active compounds

Potential as an anti-cancer agent

Yes, shows promise as a treatment for various types of cancer

Other properties

Antimicrobial and anti-inflammatory properties

Importance

Versatile and important chemical in the field of medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 54255-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,2,5 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54255-79:
(7*5)+(6*4)+(5*2)+(4*5)+(3*5)+(2*7)+(1*9)=127
127 % 10 = 7
So 54255-79-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H8ClN3O2/c14-10-6-5-8(17(18)19)7-9(10)13-15-11-3-1-2-4-12(11)16-13/h1-7H,(H,15,16)

54255-79-7SDS

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 2-(2-Chloro-5-nitrophenyl)-1H-benzimidazole

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:54255-79-7 SDS

54255-79-7Relevant articles and documents

Preparation method and application of antibacterial drugs

-

, (2020/05/02)

The invention provides phosphite ester compounds with an antibacterial effect and represented by a general formula I, a preparation method of the compounds, an application of the compounds in antibacterial drugs and pharmaceutical compositions containing the compounds. The ten synthesized compounds are novel in structure, the antibacterial activity of the compounds is equivalent to or even superior to that of positive control clindamycin and ciprofloxacin, the antibacterial spectrum is wide, and the compounds 5 and 10 are particularly expected to be further developed into antibacterial activedrugs.

N - 3 - benzimidazole thiazole derivative and its preparation method and application

-

, (2018/06/04)

The invention discloses a new compound N-3-benzimidazole thiazole amine derivative and a preparation method and application thereof. A structural formula of the compound is shown as in figure I, and in the figure I, R1 is morpholinyl, piperidyl, N-methyl piperazinyl, N-arylpiperazine, diethylin, ethyoxyl, (dimethoxy)ethylamino, or R1 is one of mono-substituted or multi-substituted aniline on the following benzene ring: fluorine, chlorine, trifluoromethoxyl, methyl, methoxyl, hydroxyl group, nitryl, amino group, acetamido, trifluoromethyl and cyano group. The compound disclosed by the invention has better antineoplastic activity, and can be used as a therapeutic agent for treating a tumor in the field of antineoplastic drug preparation.

A second group of the benzimidazole aryl amide compound and its synthesis and use

-

, (2016/12/01)

The invention relates to a diaryl amide compound containing benzimidazole group as well as the synthesis and application of the diaryl amide compound and belongs to the field of chemical medicine. The compound has a general formula I shown in the specific

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