197517-41-2

Basic information

• Product Name: 5-chloro-2-hydroxy-N-L-phenylalaninebenzamide
• Synonyms: 5-chloro-2-hydroxy-N-L-phenylalaninebenzamide
• CAS NO: 197517-41-2
• Molecular Weight: 319.744
• Mol File: 197517-41-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 5-chloro-2-hydroxy-N-L-phenylalaninebenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 5-chloro-2-hydroxy-N-L-phenylalaninebenzamide(197517-41-2)
• EPA Substance Registry System: 5-chloro-2-hydroxy-N-L-phenylalaninebenzamide(197517-41-2)

Safety Data

• Hazardous Substances Data: 197517-41-2(Hazardous Substances Data)

Upstream product

• 63-91-2 L-phenylalanine 
• 321-14-2 5-chloro-2-hydroxybenzoic acid 
• 1072896-51-5 2,5-dioxopyrrolidin-1-yl 5-chloro-2-hydroxybenzoate 
• 1734-62-9 2-acetoxy-5-chloro-benzoic acid 
• 2577-90-4 methyl (2S)-2-amino-3-phenylpropanoate 

Downstream Products

• 63-91-2 L-phenylalanine 
• 321-14-2 5-chloro-2-hydroxybenzoic acid 

Relevant articles and documents

Ochratoxin A acts as a photoactivatable DNA cleaving agent

The ability of ochratoxin A to photoinduce DNA cleavage is described; in the presence of DNA the photoreaction yields the non-chlorinated derivative, ochratoxin B, while a hydroquinone derivative is produced under anaerobic conditions.

Effect of the mimic structure on the molecular recognition properties of molecularly imprinted polymers for ochratoxin A prepared by a fragmental approach

In this work the fragmental approach was used to prepare several molecularly imprinted ethylene dimethacrylate-co-methacrylic acid polymers with molecular recognition towards the mycotoxin ochratoxin A, with the aim of searching for simpler mimic template

The synthesis of bromo- and iodo-ochratoxin B

The effective synthesis of bromo- and iodo-ochratoxin B by the treatment of ochratoxin B with pyridinium hydrobromide perbromide, and iodine and mercury(II)oxide, respectively, is reported.