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β-anilinopropionic acid anilide, also known as 3-(anilino)propionic acid anilide, is a chemical compound with the molecular formula C15H16N2O2. It is a derivative of β-anilinopropionic acid, where an aniline group (phenylamine) is attached to the propionic acid backbone. β-anilinopropionic acid anilide is characterized by its amide linkage between the carboxylic acid group of the propionic acid and the amino group of aniline. β-anilinopropionic acid anilide is a white crystalline solid and is used in various chemical and pharmaceutical applications, such as the synthesis of pharmaceuticals and as an intermediate in the production of certain drugs. It is important to note that handling and use of β-anilinopropionic acid anilide should be done with caution, as it may have potential health and environmental impacts.

79888-54-3

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79888-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79888-54-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,8 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79888-54:
(7*7)+(6*9)+(5*8)+(4*8)+(3*8)+(2*5)+(1*4)=213
213 % 10 = 3
So 79888-54-3 is a valid CAS Registry Number.

79888-54-3Relevant academic research and scientific papers

Aza-Michael reactions catalyzed by samarium diiodide

Reboule, Iréna,Gil, Richard,Collin, Jacqueline

, p. 7761 - 7764 (2007/10/03)

Samarium diiodide catalyzes the Michael addition of aromatic amines onto α,β-unsaturated N-acyloxazolidinones to form β-aminoacid derivatives. Aza-Michael reactions can be followed by an amidation reaction with the aromatic amine, leading to β-aminoamides

Electrochemical Oxidation of 1-Phenylpyrazolidin-3-ones. Part 1. 4- and 5-Substituted 1-Phenylpyrazolidin-3-ones

Bellamy, Anthony J.,Innes, David I.,Hillson, Peter J.

, p. 1599 - 1604 (2007/10/02)

The electrochemical oxidation of 4-methyl-, 5-phenyl-, and 4-hydroxymethyl-4-methyl-1-phenylpyrazolidin-3-one in acetonitrile has been studied.All three systems behave in a manner similar to that of the parent 1-phenylpyrazolidin-3-one, the major reaction

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