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238088-48-7

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238088-48-7 Usage

Structure

Contains two amino groups and a benzimidazole group

Application

Used in pharmaceutical research and drug development

Synthesis

Used in the synthesis of various biologically active molecules

Potential applications

Treatment of various diseases and disorders

Role

Used as a building block in organic synthesis

Ongoing research

Exploring potential therapeutic properties and developing new pharmaceutical agents based on its structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 238088-48-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,8,0,8 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 238088-48:
(8*2)+(7*3)+(6*8)+(5*0)+(4*8)+(3*8)+(2*4)+(1*8)=157
157 % 10 = 7
So 238088-48-7 is a valid CAS Registry Number.

238088-48-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-Benzimidazolylmethyl)ethylenediamine

1.2 Other means of identification

Product number -
Other names N1-(1H-Benzoimidazol-2-ylmethyl)-ethane-1,2-diamine

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:238088-48-7 SDS

238088-48-7Downstream Products

238088-48-7Relevant articles and documents

Synthesis of 1,2-disubstituted Δ2-imidazolines with heterylmethyl fragments

Kelarev,Koshelev,Silin

, p. 1196 - 1199 (2007/10/03)

Condensation of N-(2-thenyl)-, N-(2-benzimidazolylmethyl)- and N-(l-benzotriazolylmethyl)ethylendiamine with hydrochlorides of iminoesters of carboxylic acids affords 1,2-disubstituted Δ2-imidazolines with heteromethyl substituents in position 1.

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