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1H-Benzimidazole, 4,5,6,7-tetrahydro-2-methyl- is an organic compound with the molecular formula C9H12N2. It is a derivative of benzimidazole, a heterocyclic aromatic organic compound consisting of a benzene ring fused to an imidazole ring. The compound is characterized by its 4,5,6,7-tetrahydro structure, which means that the molecule contains four hydrogen atoms attached to the carbon atoms in the benzene ring, making it a saturated compound. Additionally, it has a methyl group (-CH3) attached to the 2-position of the benzimidazole ring. 1H-Benzimidazole, 4,5,6,7-tetrahydro-2-methyl- is known for its potential applications in pharmaceuticals and as a building block in the synthesis of various organic molecules. It is typically used as an intermediate in the preparation of more complex molecules and may have biological activity, making it a subject of interest in chemical research and drug development.

3291-07-4

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3291-07-4 Usage

Derivative of benzimidazole

bicyclic aromatic compound

Tetrahydro-2-methyl

hydrogenation of the 4,5,6,7 positions and methyl group on the 2nd carbon atom

Biological activities

diverse range of effects

Pharmacological properties

potential for antiviral, antibacterial, and antifungal applications

Medicinal chemistry and drug discovery

possible applications in these fields

Further research needed

to fully understand properties and potential uses

Check Digit Verification of cas no

The CAS Registry Mumber 3291-07-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3291-07:
(6*3)+(5*2)+(4*9)+(3*1)+(2*0)+(1*7)=74
74 % 10 = 4
So 3291-07-4 is a valid CAS Registry Number.

3291-07-4Downstream Products

3291-07-4Relevant academic research and scientific papers

A Novel Beckmann Fission Reaction of 2-Aminocyclohexanone Oxime

Sato, Haruyo,Imamura, Shinzo,Kitano, Yukishige

, p. 895 - 896 (1984)

2-(4-Cyanobutyl)-4,5,6,7-tetrahydrobenzimiazole was obtained by treating 2-aminocyclohexanone oxime with ethyl acetimidate hydrochloride in acetic acid at below 50 deg C, though only 2-methyl-4,5,6,7-tetrahydrobenzimidazole was produced by the reaction of 2-aminocyclohexanone oxime and free ethyl acetimidate in neutral solvents.A novel Beckmann fission reaction of dimeric 2-aminocyclohexanone oxime is presumed to participate in the formation of 2-(4-cyanobutyl)-4,5,6,7-tetrahydrobenzimidazole.

SUBSTITUTED PYRIDINE AND PYRAZINE BMI-1 INHIBITORS

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Page/Page column 203, (2015/06/08)

Amine substituted pyridine and pyrazine compounds and forms thereof that inhibit the function and reduce the level of B -cell specific Moloney murine leukemia virus integration site 1 (Bmi-1) protein and methods for their use to inhibit Bmi-1 function and reduce the level of Bmi-1 to treat a cancer mediated by Bmi-1 are described herein.

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