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1837-49-6

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1837-49-6 Usage

General Description

1-Methyl-4,5,6,7-tetrahydro-1H-benzimidazole is a chemical compound that belongs to the benzimidazole class of compounds. It is a heterocyclic compound consisting of a benzene ring fused to an imidazole ring. This chemical is used in various applications, including as a building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It has also been studied for its potential biological activities, including its role as a dopamine receptor agonist. Additionally, it may have potential uses as a ligand in metal coordination chemistry. Studies have shown this compound to possess various pharmacological activities, including anti-inflammatory, anti-cancer, and anti-microbial properties. Overall, 1-Methyl-4,5,6,7-tetrahydro-1H-benzimidazole is a versatile compound with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1837-49-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,3 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1837-49:
(6*1)+(5*8)+(4*3)+(3*7)+(2*4)+(1*9)=96
96 % 10 = 6
So 1837-49-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2/c1-10-6-9-7-4-2-3-5-8(7)10/h6H,2-5H2,1H3

1837-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-4,5,6,7-tetrahydrobenzimidazole

1.2 Other means of identification

Product number -
Other names N-methyltetrahydrobenzimidazole

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:1837-49-6 SDS

1837-49-6Upstream product

1837-49-6Relevant articles and documents

Process for producing epsilon-caprolactam

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Paragraph [0056] - [0059], (2008/06/13)

A high purity ε-caprolactam is prepared by pouring a molten crude ε-caprolactam and a solvent comprising an aliphatic hydrocarbon and having a lower temperature than that of the crude ε-caprolactam, into a vessel and mixing them to obtain a first slurry containing a crystallized ε-caprolactam. The slurry is then subjected to a solid-liquid separation to obtain ε-caprolactam and a first liquid phase. This process can effectively remove impurities from a crude ε-caprolactam, which is obtained by for example, subjecting cyclohexanone oxime to the Beckmann rearrangement.

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