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68426-81-3

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68426-81-3 Usage

Structure

Benzimidazole ring with an attached ethenyl group and a methyl and methoxy substituent

Usage

Research and pharmaceutical applications due to potential biological activities

Studied for

Anticancer, antimicrobial, and antifungal properties

Potential

Promising candidate for further drug development

Applications

Synthesis of new organic compounds and materials (however, further research is needed)

Check Digit Verification of cas no

The CAS Registry Mumber 68426-81-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,4,2 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 68426-81:
(7*6)+(6*8)+(5*4)+(4*2)+(3*6)+(2*8)+(1*1)=153
153 % 10 = 3
So 68426-81-3 is a valid CAS Registry Number.

68426-81-3SDS

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 1H-Benzimidazole,2-ethenyl-5-methoxy-1-methyl-(9CI)

1.2 Other means of identification

Product number -
Other names 5-Methoxy-1-methyl-3,4-dihydro-1H-naphthalin-2-on

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:68426-81-3 SDS

68426-81-3Downstream Products

68426-81-3Relevant articles and documents

Aryl radical cyclisation onto pyrroles

Escolano, Carmen,Jones, Keith

, p. 1453 - 1464 (2007/10/03)

The intramolecular cyclisation of aryl radicals onto a pyrrole is studied. The cyclisation allows the synthesis of either the spiropyrrolidinyloxindole or the pyrrolo[3,2-c]quinoline skeleton depending on the nature of the protecting group at the N-pyrrole atom. The regiochemistry of the cyclisation is not affected by the substituents on the benzene ring. Some limitations on the utility of tosylmethylisocyanide in pyrrole synthesis are also reported.

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