1155-48-2

Basic information

• Product Name: 2-(benzoylamino)-3-phenylprop-2-enoic acid
• CAS NO: 1155-48-2
• Molecular Formula: C₁₆H₁₃NO₃
• Molecular Weight: 267.2793
• Mol File: 1155-48-2.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 520.4°C at 760 mmHg
• Flash Point: 268.6°C
• Density: 1.275g/cm³
• Vapor Pressure: 1.17E-11mmHg at 25°C
• Refractive Index: 1.653
• CAS DataBase Reference: 2-(benzoylamino)-3-phenylprop-2-enoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(benzoylamino)-3-phenylprop-2-enoic acid(1155-48-2)
• EPA Substance Registry System: 2-(benzoylamino)-3-phenylprop-2-enoic acid(1155-48-2)

Safety Data

• Hazardous Substances Data: 1155-48-2(Hazardous Substances Data)

Usage

General Description

2-(benzoylamino)-3-phenylprop-2-enoic acid is a chemical compound with the molecular formula C17H15NO3. It is a derivative of the amino acid phenylalanine, with a benzoylamino group attached to the amino group. 2-(benzoylamino)-3-phenylprop-2-enoic acid is commonly referred to as Benzoylphenylalanine, and is used in research and pharmaceutical applications. It has been studied for its potential role in inhibiting the growth of cancer cells, as well as its potential use in drug delivery systems. Its chemical structure and properties make it an interesting and potentially useful compound for further research and development.

Upstream product

• 842-74-0 4-benzylidene-2-phenyloxazole-5(4H)-one 
• 26348-47-0 (Z)-2-benzamidocinnamic acid 
• 356791-01-0 N-(1-oxo-3-phenyl-1-(piperidin-1-yl)-prop-2-en-2-yl)benzamide 
• 18510-92-4 N-hydroxy-3,N-diphenyl-2-thiobenzoylamino-acrylamide 
• 16446-30-3 4-benzylidene-2-phenyl-4H-thiazol-5-one 
• 100-52-7 benzaldehyde 
• 17606-70-1 (4Z)-4-benzylidene-2-phenyl-1,3-oxazol-5(4H)-one 
• 32089-78-4 ethyl 2-(benzoylamino)-3-(phenyl)acrylate 
• 18510-74-2 4-benzylidene-2,6-diphenyl-4H-[1,2,5]oxadiazin-3-one 
• 21462-02-2 methyl (Z)-2-benzoylamino-3-phenyl-2-propenoate 
• 15732-43-1 (E)-2-phenyl-4-benzylidene-5(4H)-oxazolone 
• 27573-05-3 methyl ester of benzoylaminocinnamic acid 

Downstream Products

• 156-06-9 2-oxo-3-(phenyl)propionic acid 
• 55-21-0 benzamide 
• 150-30-1 Phenylalanine 
• 6362-70-5 5-benzyl-4-phenyl-dihydro-furan-2,3-dione 
• 2566-22-5 DL-N-benzoylphenylalanine 
• 83556-31-4 Phac-DL-Phe-NH₂ 
• 23912-50-7 N-benzoyl-phenylalanine hydrazide 
• 17606-70-1 (4Z)-4-benzylidene-2-phenyl-1,3-oxazol-5(4H)-one 
• 153199-75-8 ethyl (1-benzoylamino-2-phenylethenyl)phenylphosphinate 
• 2566-22-5 N-benzoyl-L-phenylalanine 
• 37002-52-1 N-benzoyl-D-phenylalanine 
• 842-74-0 4-benzylidene-2-phenyloxazole-5(4H)-one 
• 144264-38-0 2-Benzoylamino-2,3-dichloro-3-phenyl-propionic acid 
• 132649-36-6 2-benzoylamino-3-phenyl-3-chloroacrylic acid 

Relevant articles and documents

Reaction of 2-Phenyl-4-arylidene-1,3-oxazolones with Different Nucleophiles for Synthesis of Some New Heterocycles

Refluxing of 1,3-oxazolone (1a) with malononitrile in dry benzene and in the presence of ammonium acetate afforded imidazolone derivative (2). However, carrying out the same reaction in absolute ethanol and in the presence of piperidine as a base gave the

Physical characteristics and polarographic reduction mechanism of some oxazolones

The redox potential (ΔE1/2), electron affinity (EA), ionization potential (IP), coulomb repulsion integral (J12), and electronic transition energy (ECT) of several oxazolone derivatives in DMF were computed.A linear correlation was shown to exist between ΔE1/2 and ECT.The polarographic reduction was investigated in ethanolic-Theil buffer solutions.At pH /= 7.2, two waves were obtained representing the uptake of 2- and 4-electron steps respectively.In alkaline media, a third wave appeared seemingly a result of the hydrolysis of oxazolones.The rate of hydrolysis was determined and the electrode mechanism was elucidated and confirmed via spectrophotometric and coulometric analysis. Key words: oxazolones, polarography, electrochemistry, electrode reaction, spectrophotometry, redox potential.

SOME REMARKS CONCERNING THE PUBLICATION 'A NOVEL SYNTHESIS OF 3-SUBSTITUTED PYRUVIC ACIDS; A NEW ROUTE TO α,β-DIAMINO ACIDS' BY M.M. KIDWAI, N.H. KHAN AND M. ALI

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