94460-79-4

Basic information

• Product Name: DL-2-Benzamino-3-(4-hydroxy-phenyl)-propan-1-ol; 'N-Benzoyl-DL-tyrosinol'
• CAS NO: 94460-79-4
• Molecular Weight: 271.316
• Mol File: 94460-79-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: DL-2-Benzamino-3-(4-hydroxy-phenyl)-propan-1-ol; 'N-Benzoyl-DL-tyrosinol'(CAS DataBase Reference)
• NIST Chemistry Reference: DL-2-Benzamino-3-(4-hydroxy-phenyl)-propan-1-ol; 'N-Benzoyl-DL-tyrosinol'(94460-79-4)
• EPA Substance Registry System: DL-2-Benzamino-3-(4-hydroxy-phenyl)-propan-1-ol; 'N-Benzoyl-DL-tyrosinol'(94460-79-4)

Safety Data

• Hazardous Substances Data: 94460-79-4(Hazardous Substances Data)

Upstream product

• 1226-71-7 4-(4-hydroxybenzylidene)-2-phenyloxazol-5(4H)-one 
• 34996-91-3 N-benzoyl-(4'-hydroxy)phenylalanine 
• 4276-17-9 methyl (N-benzoyl)-4'-hydroxyphenylalaninate 

Downstream Products

• 500-88-9 (+/-)-2-amino-3-(4-hydroxyphenyl)-1-propanol 

Relevant articles and documents

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.