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β-Butyl-N-(2-methylphenyl)benzenepropanamide is a complex organic compound with the chemical formula C20H23NO. It is a derivative of benzenepropanamide, featuring a butyl group (C4H9) attached to the β-carbon of the propane chain, and a 2-methylphenyl group (C7H7) connected to the nitrogen atom. β-butyl-N-(2-methylphenyl)benzenepropanamide is characterized by its long, flexible molecular structure, which allows for various conformations and interactions with other molecules. It is primarily used in the pharmaceutical industry as an intermediate in the synthesis of various drugs, particularly those targeting the central nervous system. Due to its specific structure, it can interact with biological receptors, potentially modulating their activity and leading to therapeutic effects.

78987-22-1

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78987-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78987-22-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,8 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78987-22:
(7*7)+(6*8)+(5*9)+(4*8)+(3*7)+(2*2)+(1*2)=201
201 % 10 = 1
So 78987-22-1 is a valid CAS Registry Number.

78987-22-1Downstream Products

78987-22-1Relevant academic research and scientific papers

Lithiation of N-(2-Alkylphenyl)alkanamides and Related Compounds. A Modified Madelung Indole Synthesis

Houlihan, William J.,Parrino, Vincent A.,Uike, Yasuyuki

, p. 4511 - 4515 (2007/10/02)

A modified Madelung synthesis for the conversion of N-(alkylphenyl)alkanamides and related compounds to indoles, benzindoles, and azindoles has been developed.This procedure consists of treating the amide with 2 or 3 equiv of n-butyllithium or lithium diisopropylamide in tetrahydrofuran at temperatures from -20 to +25 deg C.Several examples where products other than indoles were formed from the starting amide are also reported.

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