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1H-Benzimidazole,2-(ethoxymethyl)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80761-36-0

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80761-36-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80761-36-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,6 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 80761-36:
(7*8)+(6*0)+(5*7)+(4*6)+(3*1)+(2*3)+(1*6)=130
130 % 10 = 0
So 80761-36-0 is a valid CAS Registry Number.

80761-36-0SDS

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 2-(Ethoxymethyl)-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 2-Aethoxymethyl-1H-benzimidazol

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:80761-36-0 SDS

80761-36-0Downstream Products

80761-36-0Relevant academic research and scientific papers

A unique one-pot reaction via CC cleavage from aminomethylene benzimidazoles to access benzimidazolones with wide potentiality

Zhang, Hui-Zhen,Cui, Sheng-Feng,Nagarajan, Sangaraiah,Rasheed, Syed,Cai, Gui-Xin,Zhou, Cheng-He

supporting information, p. 4105 - 4109 (2014/07/22)

A unique one-pot reaction via CC cleavage from aminomethylene benzimidazoles with commercial halides to access novel benzimidazolones is reported for the first time. The previously unexploited transformation is able to perform smoothly in the presence of

Design, synthesis, and evaluation of novelly substituted benzimidazole compounds as angiotensin II receptor antagonists

Bali, Alka,Bansal, Yogita,Sugumaran,Saggu, Jatinder Singh,Balakumar,Kaur, Gurpreet,Bansal, Gulshan,Sharma, Ajay,Singh, Manjeet

, p. 3962 - 3965 (2007/10/03)

5-Nitrobenzimidazole derivatives with varying substituents at 2-position have been designed, synthesized, and evaluated for angiotensin II antagonistic activity. A drug-receptor interaction model has been proposed.

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