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2-(α-hydroxybenzyl)-5(6)-nitrobenzimidazole is a complex organic compound with the molecular formula C14H11N3O3. It is a derivative of benzimidazole, featuring a nitro group at the 5th or 6th position and an α-hydroxybenzyl substituent at the 2nd position. 2-(α-hydroxybenzyl)-5(6)-nitrobenzimidazole is known for its potential applications in medicinal chemistry, particularly as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its structure allows for the exploration of its biological activities, such as antimicrobial, antiviral, and anticancer properties, due to its ability to interact with DNA and other biological targets. The compound's synthesis and functionalization are of interest to researchers looking to develop new therapeutic agents and understand its mechanism of action.

5086-55-5

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5086-55-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5086-55-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,8 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5086-55:
(6*5)+(5*0)+(4*8)+(3*6)+(2*5)+(1*5)=95
95 % 10 = 5
So 5086-55-5 is a valid CAS Registry Number.

5086-55-5Downstream Products

5086-55-5Relevant academic research and scientific papers

Practicable Syntheses of 2-Hydroxymethyl-substituted Benzimidazoles and 2-Formylbenzimidazole

Ooi, Hong Chin,Suschitzky, Hans

, p. 2871 - 2876 (2007/10/02)

N-Protection of benzimidazole by a diethoxymethyl group, as in , allows exclusive lithiation at the 2-position.This protected anion can be made to react with various electrophiles (e. g. ketones, aldehydes) to yield the corresponding 2-hydroxymethylbenzimidazoles (1).Facile deprotection occurs with acid.Two practicable syntheses of 2-formylbenzimidazole are also described and an indirect route to benzimidazole-2-alcohols is discussed.

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