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102169-73-3

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102169-73-3 Usage

Chemical Class

Benzimidazoles

Derivative

1H-Benzimidazole-5,6-diol(9CI)

Hydroxyl groups

Located at positions 5 and 6 on the benzene ring

Pharmaceutical applications

Potential use in drug development

Biological activities

Antioxidant, anti-inflammatory, potential antitumor and antiviral activities

Ongoing research

Exploration of its potential in the development of new drugs for various therapeutic purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 102169-73-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,1,6 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 102169-73:
(8*1)+(7*0)+(6*2)+(5*1)+(4*6)+(3*9)+(2*7)+(1*3)=93
93 % 10 = 3
So 102169-73-3 is a valid CAS Registry Number.

102169-73-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-benzimidazole-5,6-diol

1.2 Other means of identification

Product number -
Other names 5,6-Benzimidazolediol(6CI)

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:102169-73-3 SDS

102169-73-3Downstream Products

102169-73-3Relevant articles and documents

Expanding the aqueous-based redox-facilitated self-polymerization chemistry of catecholamines to 5,6-dihydroxy-1H-benzimidazole and its 2-substituted derivatives

Fan, Ka Wai,Peterson, Matthew B.,Ellersdorfer, Peter,Granville, Anthony M.

, p. 25203 - 25214 (2016/03/22)

Aqueous-base redox-facilitated self-polymerization can be performed with 5,6-dihydroxy-1H-benzimidazole (DHBI) to generate polymeric material that is analogous to poly(dopamine) (PDA), proving the possibility to expand the catecholamine-exclusive chemistr

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