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(1-ethyl-1H-benzoimidazol-2-yl)-phenyl-methanol is a complex organic compound with the molecular formula C17H17N2O. It is characterized by a benzoimidazole ring, which is fused to a phenyl group, and an ethyl group attached to the nitrogen atom. The molecule also features a phenylmethanol moiety, indicating the presence of a hydroxyl group (-OH) attached to a benzene ring. This chemical is known for its potential applications in the pharmaceutical industry, particularly as a building block for the synthesis of various bioactive molecules. Its structure provides a foundation for further chemical modifications, which can lead to the development of new drugs with specific therapeutic properties.

3785-64-6

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3785-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3785-64-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,8 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3785-64:
(6*3)+(5*7)+(4*8)+(3*5)+(2*6)+(1*4)=116
116 % 10 = 6
So 3785-64-6 is a valid CAS Registry Number.

3785-64-6Downstream Products

3785-64-6Relevant academic research and scientific papers

Synthesis and in vitro antifungal evaluation of benzoimidazolyl-piperazinyl-phenylmethanone derivatives

Kankate, Rani S.,Gide, Parag S.,Belsare, Deepak P.

, p. 1855 - 1863 (2015/04/22)

Benzimidazole and piperazines are the important pharmacophores in the structures of many antifungal compounds. Further, the phenylmethanone are also a unique class of compounds whose antifungal profile is not much exploited. So to exploit their antifungal potential we have selected these three combinations and framed the novel parent structure for our research work. In this study a novel series of benzimidazoles derivatives was synthesized by microwave irradiation and characterized by 1H NMR, 13C NMR, Infra Red (IR), and Mass Spectroscopy (MS), and by elemental analysis. The screening of compound for in vitro (turbidimetric method) antifungal activity against C.albicans revealed activity in many of the compounds as comparable to that of ketoconazole.

Alternate method for the synthesis of N-alkyl/aralkyl-2-(α-hydroxy alkyl/aralkyl)benzimidazoles via regiospecific acetylation

Dubey,Reddy, P.V.V. Prasada,Srinivas

, p. 1675 - 1681 (2008/02/01)

Acetylation of 1H-2-(α-hydroxyalkyl/aryl)benzimidazoles 2 with Ac2O results in the regiospecific formation of O-acetoxy derivative 3, which on alkylation with alkylating agents in nonaqueous media under phase-transfer catalytic conditions affords N-alkyl

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