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34734-20-8

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34734-20-8 Usage

Structure

Fused heterocyclic compound with a benzene ring fused to an imidazole ring

Functional groups

Carboxaldehyde and ethyl substituent

Carboxaldehyde group

Present at the 2nd position of the benzimidazole ring

Ethyl substituent

Attached to the nitrogen atom in the imidazole ring

Applications

Pharmaceutical and industrial uses as a building block for organic synthesis

Potential uses

Being studied for biological activities and therapeutic applications

Safety precautions

Handle with care due to potential hazards associated with its use

Check Digit Verification of cas no

The CAS Registry Mumber 34734-20-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,7,3 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 34734-20:
(7*3)+(6*4)+(5*7)+(4*3)+(3*4)+(2*2)+(1*0)=108
108 % 10 = 8
So 34734-20-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O/c1-2-12-9-6-4-3-5-8(9)11-10(12)7-13/h3-7H,2H2,1H3

34734-20-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethylbenzimidazole-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1-Ethylbenzimidazol-2-aldehyd

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:34734-20-8 SDS

34734-20-8Relevant articles and documents

Condensation reactions of vinyl and ethyl derivatives of 2-amino-and 2-formylimidazoles

Balkalova,Domnina,Chipanina,Afonin,Shulunova

, p. 962 - 966 (2007/10/03)

New Schiff bases of 1-vinyl-and 1-ethyl-substituted imidazoles and benzimidazoles were synthesized. The condensation reactions of 2-amino-and 2-formylimidazoles with 2-aminobenzimidazoles are virtually independent of the nature of the substituent (CH=CH2 or Et) at position 1 of the heterocycle. The structures of the azomethines synthesized were established by 1H NMR and IR spectroscopy.

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