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Phenylmercapto-essigsaeure-homoveratrylamid, also known as 3-(4-aminophenyl)-3-phenylpropanenitrile, is a complex organic chemical compound with the molecular formula C15H14N2. It is a derivative of veratrylamine, which is an aromatic amine, and features a phenylmercapto group (a sulfur-containing phenyl group) and an acetic acid moiety. Phenylmercapto-essigsaeure-homoveratrylamid is characterized by its unique structure, which combines the properties of an amine, a phenyl group, and a mercaptan. It is synthesized through a series of chemical reactions and is used in various applications, including as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Due to its specific functional groups, it may exhibit unique chemical reactivity and properties, making it a subject of interest in organic chemistry research.

5597-12-6

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5597-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5597-12-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,9 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5597-12:
(6*5)+(5*5)+(4*9)+(3*7)+(2*1)+(1*2)=116
116 % 10 = 6
So 5597-12-6 is a valid CAS Registry Number.

5597-12-6Relevant academic research and scientific papers

An efficient synthesis of γ-substituted α,β-unsaturated-δ-lactams. Formal synthesis of (±)-protoemetinol

Huang, Chang-Gin,Chang, Bo-Rui,Chang, Nein-Chen

, p. 2721 - 2723 (2002)

γ-Substituted α,β-unsaturated δ-lactams 1 was synthesized from α-sulfinyl acetamides 3 in three steps. Formal synthesis of (±)-protoemetinol was also reported.

Syntheses of 2-(3,4-dimethoxyphenyl)ethylamine derivatives and their antiulcer activities

Hosokami,Kuretani,Higashi,Asano,Ohya,Takasugi,Mafune,Miki

, p. 2712 - 2719 (2007/10/02)

A series of acyl derivatives of 2-(3,4-dimethoxyphenyl)ethylamine (4) were synthesized and evaluated for their effectiveness to prevent water-immersion stress-induced gastric ulceration when given intraperitoneally to rats. Among them N-[2-(3,4-dimethoxyp

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