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116121-25-6

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116121-25-6 Usage

Class

Organic compound, benzimidazole derivative

Appearance

White to light yellow crystalline solid

Use

Building block for the synthesis of various pharmaceutical compounds

Biological activity

Potential as an antiviral, anti-tumor, and antifungal agent

Structure

Benzimidazole ring system with an amine and phenyl group attached

Check Digit Verification of cas no

The CAS Registry Mumber 116121-25-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,2 and 1 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 116121-25:
(8*1)+(7*1)+(6*6)+(5*1)+(4*2)+(3*1)+(2*2)+(1*5)=76
76 % 10 = 6
So 116121-25-6 is a valid CAS Registry Number.

116121-25-6SDS

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 1-ethyl-N-phenylbenzimidazol-2-amine

1.2 Other means of identification

Product number -
Other names 1H-Benzimidazol-2-amine,1-ethyl-N-phenyl

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:116121-25-6 SDS

116121-25-6Downstream Products

116121-25-6Relevant articles and documents

CONDENSED DERIVATIVES OF BENZAZOLES. 1. SYNTHESIS OF 6- AND 5-SUBSTITUTED BENZIMIDAZOQUINAZOLIN-12-ONES

Popov, I. I.,Boroshko, S. L.,Tertov, B. A.,Makarov, S. P.,Simonov, A. M.,Simkin, B. Ya.

, p. 1348 - 1352 (2007/10/02)

6(5)H-Benzimidazoquinazolin-12-one was obtained in high yield by condensation of benzimidazole-2-sulfonic acid with anthranilic acid.Methods for the introduction of substituents selectively into the 5 and 6 positions of this heterocycle were develo

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