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1H-Benzimidazole, 2-(3-cyclohexylpropyl)- is an organic compound with the molecular formula C14H20N2. It is a derivative of benzimidazole, a heterocyclic aromatic organic compound consisting of a benzene ring fused to an imidazole ring. The 2-(3-cyclohexylpropyl) substitution refers to the presence of a cyclohexylpropyl group attached to the benzimidazole core at the 2-position. 1H-Benzimidazole, 2-(3-cyclohexylpropyl)- is known for its potential applications in pharmaceuticals and chemical research, particularly in the development of new drugs and as a building block for more complex molecules. Its unique structure allows for a range of chemical reactions and interactions, making it a valuable compound in the field of organic chemistry.

1087-17-8

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1087-17-8 Usage

Chemical class

benzimidazole

Structure

a benzene ring fused to an imidazole ring, with a cyclohexylpropyl group attached at the 2-position of the imidazole ring

Usage

commonly used in the pharmaceutical industry for the development of drugs targeting various diseases and conditions

Value

unique structure and properties make it a valuable building block for the synthesis of biologically active molecules and potential drug candidates

Modulation

the 3-cyclohexylpropyl moiety can modulate the pharmacological properties of the compounds, making it a versatile chemical for medicinal chemistry research.

Check Digit Verification of cas no

The CAS Registry Mumber 1087-17-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,8 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1087-17:
(6*1)+(5*0)+(4*8)+(3*7)+(2*1)+(1*7)=68
68 % 10 = 8
So 1087-17-8 is a valid CAS Registry Number.

1087-17-8Downstream Products

1087-17-8Relevant academic research and scientific papers

Synthesis and tuberculostatic activity of new benzimidazole derivatives

Foks,Pancechowska-Ksepko,Kuzmierkiewicz,Zwolska,Augustynowicz-Kopec,Janowiec

, p. 611 - 614 (2006)

The reactions of o-phenylenediamine and 3,4-diaminotoluene with such acids as 3-cyclohexylpropionic, 4-phenylbutyric, 4-cyclohexylbutyric, 3,3-diphenylpropionic, and 3,4-dimethoxyphenylacetic resulted in the formation of the corresponding 2-substituted be

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