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
1837-49-6Relevant 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.