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1H-Benzimidazol-6-amine, N,N-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1262887-26-2

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1262887-26-2 Usage

Structure

Derivative of benzimidazole with a benzene and imidazole ring

Substitution

Two methyl (CH3) groups attached to the nitrogen atom on the benzimidazole ring

Potential applications

Building block in organic synthesis, pharmaceutical intermediate, reagent in chemical research

Utility

Useful in the development of new materials or in the production of pharmaceuticals, development of new drugs, or biochemical research

Unique aspects

Benzimidazole structure and nitrogen substitution with methyl groups

Check Digit Verification of cas no

The CAS Registry Mumber 1262887-26-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,8,8 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1262887-26:
(9*1)+(8*2)+(7*6)+(6*2)+(5*8)+(4*8)+(3*7)+(2*2)+(1*6)=182
182 % 10 = 2
So 1262887-26-2 is a valid CAS Registry Number.

1262887-26-2SDS

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 N,N-dimethyl-1H-benzo[d]imidazol-6-amine

1.2 Other means of identification

Product number -
Other names -

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:1262887-26-2 SDS

1262887-26-2Downstream Products

1262887-26-2Relevant academic research and scientific papers

Mild and general one-pot reduction and cyclization of aromatic and heteroaromatic 2-nitroamines to bicyclic 2 H -imidazoles

Hanan, Emily J.,Chan, Bryan K.,Estrada, Anthony A.,Shore, Daniel G.,Lyssikatos, Joseph P.

, p. 2759 - 2764 (2010)

A one-pot procedure for the conversion of aromatic and heteroaromatic 2-nitroamines into bicyclic 2H-benzimidazoles is described. The procedure employs formic acid, iron powder, and an additive such as NH4Cl to reduce the nitro group and effect the imidazole cyclization with high-yielding conversions generally within one to two hours. The compatibility with a wide range of functionality demonstrates the general utility of this procedure.

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