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Ethanol, 2-[(1-methyl-1H-benzimidazol-2-yl)amino](9CI), also known as mebendazole, is a chemical compound with the molecular formula C11H14N2O. It is a derivative of benzimidazole, a heterocyclic compound that contains a fusion of benzene and imidazole rings. Mebendazole is used as an anthelmintic agent to treat parasitic infections in humans and animals.
Used in Pharmaceutical Industry:
Ethanol, 2-[(1-methyl-1H-benzimidazol-2-yl)amino](9CI) is used as an anthelmintic agent for treating parasitic infections in humans and animals. It works by interfering with the synthesis of microtubules in the parasites, leading to their immobilization and eventual death. Mebendazole has a wide spectrum of activity against gastrointestinal nematodes, including roundworms, whipworms, and hookworms.
Used in Cancer Research:
Ethanol, 2-[(1-methyl-1H-benzimidazol-2-yl)amino](9CI) has been studied for its potential anticancer properties. It has shown promising results in inhibiting the growth of cancer cells, making it a valuable compound for further research and development in the field of oncology.

57262-39-2

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57262-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57262-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,2,6 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57262-39:
(7*5)+(6*7)+(5*2)+(4*6)+(3*2)+(2*3)+(1*9)=132
132 % 10 = 2
So 57262-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H13N3O/c1-13-9-5-3-2-4-8(9)12-10(13)11-6-7-14/h2-5,14H,6-7H2,1H3,(H,11,12)

57262-39-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(1-methylbenzimidazol-2-yl)amino]ethanol

1.2 Other means of identification

Product number -
Other names 2,6-DICHLORO-3-NITROBENZONITRILE

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:57262-39-2 SDS

57262-39-2Relevant academic research and scientific papers

Synthesis and antiinflammatory properties of 2-aminobenzimidazole derivatives

Da Settimo,Primofiore,Da Settimo,Marini

, p. 1293 - 1313 (2007/10/02)

Several 1-alkyl or 1-aralkyl substituted 2-aminobenzimidazole derivatives, bearing an acetic or acetohydroxamic group at 3-position, were synthesized. Some of these products were tested for their antiinflammatory and analgesic properties. These compounds exhibited an antiinfammatory activity lower than that of reference drug Indomethacin. Compound 2e showed the highest efficacy, but not in a dose-related manner. Only compounds 3a and 16 exhibited some analgesic activity, but at a very high dose.

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