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2-(3,5-dimethyl-phenoxymethyl)-1H-benzoimidazole is a complex organic compound with the molecular formula C16H15N2O. It features a benzoimidazole core, which is a fused ring system consisting of a benzene ring and an imidazole ring. The compound is characterized by the presence of a 3,5-dimethylphenoxy group attached to the benzoimidazole through a methylene bridge. The dimethylphenoxy group consists of a phenol moiety with two methyl groups at the 3rd and 5th positions, which contributes to the compound's lipophilic nature. This chemical structure endows the compound with potential applications in various fields, such as pharmaceuticals, agrochemicals, or as a precursor in the synthesis of other complex molecules. Its specific properties and reactivity are influenced by the electronic and steric effects of the substituents on the aromatic rings.

3156-29-4

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3156-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3156-29-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,5 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3156-29:
(6*3)+(5*1)+(4*5)+(3*6)+(2*2)+(1*9)=74
74 % 10 = 4
So 3156-29-4 is a valid CAS Registry Number.

3156-29-4Downstream Products

3156-29-4Relevant academic research and scientific papers

Inhibition of Rat Hepatic Microsomal Aminopyrine N-Demethylase Activity by Benzimidazole Derivatives. Quantitative Structure-Activity Relationships

Murray, Michael,Ryan, Adrian J.,Little, Peter J.

, p. 887 - 892 (1982)

Eighty-two benzimidazole derivatives have been prepared and tested for the ability to inhibit cytochrome P-450 mediated enzyme activity (aminopyrine N-demethylase) from phenobarbitone-induced rat hepatic microsomes.Using physicochemical parameters and multiple regression analysis, we derived a quantitative structure-activity relationship (QSAR) that describes up to 87percent of the data variance in terms of hydrophobic and electronic effects and the molar refractivity of the substituent in the 2-position of the benzimidazole ring.

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