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5-[(3,4-dimethoxy-benzyl)-methyl-amino]-2-(3,4-dimethoxy-phenyl)-2-isopropylpentanenitrile is a complex organic compound with a molecular formula of C24H32N2O4. It is characterized by the presence of two 3,4-dimethoxyphenyl groups, a benzyl-methyl-amino group, and an isopropylpentanenitrile chain. 5-[(3,4-dimethoxy-benzyl)-methyl-amino]-2-(3,4-dimethoxy-phenyl)-2-isopropylpentanenitrile is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of certain drugs. Its structure features a nitrogen atom bonded to a benzyl group, which is further connected to a dimethoxyphenyl group, and a cyano group attached to an isopropylpentane chain. The compound's unique structure and properties make it a subject of interest for researchers in the field of medicinal chemistry.

62-71-5

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62-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62-71-5 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 6 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62-71:
(4*6)+(3*2)+(2*7)+(1*1)=45
45 % 10 = 5
So 62-71-5 is a valid CAS Registry Number.

62-71-5Downstream Products

62-71-5Relevant academic research and scientific papers

Synthesis of new verapamil analogues and their evaluation in combination with rifampicin against Mycobacterium tuberculosis and molecular docking studies in the binding site of efflux protein Rv1258c

Singh, Kawaljit,Kumar, Malkeet,Pavadai, Elumalai,Naran, Krupa,Warner, Digby F.,Ruminski, Peter G.,Chibale, Kelly

, p. 2985 - 2990 (2014/06/24)

New verapamil analogues were synthesized and their inhibitory activities against Mycobacterium tuberculosis H37Rv determined in vitro alone and in combination with rifampicin (RIF). Some analogues showed comparable activity to verapamil and exhibited better synergies with RIF. Molecular docking studies of the binding sites of Rv1258c, a M. tuberculosis efflux protein previously implicated in intrinsic resistance to RIF, suggested a potential rationale for the superior synergistic interactions observed with some analogues.

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