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1-METHYL-4,5,6,7-TETRAHYDRO-1H-BENZIMIDAZOLE is a heterocyclic chemical compound belonging to the benzimidazole class. It features a benzene ring fused to an imidazole ring, making it a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. 1-METHYL-4,5,6,7-TETRAHYDRO-1H-BENZIMIDAZOLE has been studied for its potential biological activities, such as acting as a dopamine receptor agonist, and may also be utilized as a ligand in metal coordination chemistry. It has demonstrated pharmacological properties, including anti-inflammatory, anti-cancer, and anti-microbial effects.

1837-49-6

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1837-49-6 Usage

Uses

Used in Pharmaceutical Industry:
1-METHYL-4,5,6,7-TETRAHYDRO-1H-BENZIMIDAZOLE is used as a building block in the synthesis of various pharmaceuticals for its potential role in creating new drugs with diverse therapeutic applications.
Used in Agrochemical Industry:
1-METHYL-4,5,6,7-TETRAHYDRO-1H-BENZIMIDAZOLE is used as a building block in the synthesis of agrochemicals, contributing to the development of new pesticides or other agricultural products to improve crop protection and yield.
Used in Organic Synthesis:
1-METHYL-4,5,6,7-TETRAHYDRO-1H-BENZIMIDAZOLE is used as a versatile building block in organic synthesis for creating a wide range of organic compounds with different applications in various industries.
Used in Biological Research:
As a dopamine receptor agonist, 1-METHYL-4,5,6,7-TETRAHYDRO-1H-BENZIMIDAZOLE is used in biological research to study its potential effects on neurological processes and the development of treatments for related conditions.
Used in Metal Coordination Chemistry:
1-METHYL-4,5,6,7-TETRAHYDRO-1H-BENZIMIDAZOLE is used as a ligand in metal coordination chemistry, which may lead to the development of new materials with specific properties for various applications, such as catalysis or sensing.
Used in Anti-inflammatory Applications:
1-METHYL-4,5,6,7-TETRAHYDRO-1H-BENZIMIDAZOLE is used for its anti-inflammatory properties, potentially contributing to the development of treatments for inflammatory diseases.
Used in Anti-cancer Applications:
1-METHYL-4,5,6,7-TETRAHYDRO-1H-BENZIMIDAZOLE is used for its anti-cancer properties, showing promise in the development of new cancer therapies.
Used in Anti-microbial Applications:
1-METHYL-4,5,6,7-TETRAHYDRO-1H-BENZIMIDAZOLE is used for its anti-microbial properties, which may aid in the development of new antibiotics or antifungal agents.

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 academic research and scientific papers

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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