160538-38-5

Basic information

• Product Name: methyl (S)-2-(((benzyloxy)carbonyl)amino)-3-(3,5-dibromo-4-hydroxyphenyl)propanoate
• Synonyms: methyl (S)-2-(((benzyloxy)carbonyl)amino)-3-(3,5-dibromo-4-hydroxyphenyl)propanoate
• CAS NO: 160538-38-5
• Molecular Weight: 487.145
• Mol File: 160538-38-5.mol

Chemical Properties

• CAS DataBase Reference: methyl (S)-2-(((benzyloxy)carbonyl)amino)-3-(3,5-dibromo-4-hydroxyphenyl)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (S)-2-(((benzyloxy)carbonyl)amino)-3-(3,5-dibromo-4-hydroxyphenyl)propanoate(160538-38-5)
• EPA Substance Registry System: methyl (S)-2-(((benzyloxy)carbonyl)amino)-3-(3,5-dibromo-4-hydroxyphenyl)propanoate(160538-38-5)

Safety Data

• Hazardous Substances Data: 160538-38-5(Hazardous Substances Data)

Upstream product

• 67470-21-7 3',5'-dibromo-L-tyrosine methyl ester 
• 501-53-1 benzyl chloroformate 
• 60-18-4 L-tyrosine 
• 13512-31-7 N-(benzyloxycarbonyl)-L-tyrosine methyl ester 

Downstream Products

• 113311-35-6 H-Isodityr-OMe 
• 83118-65-4 Isodityrosine 
• 160538-39-6 (S)-2-Benzyloxycarbonylamino-3-{4-[5-((S)-2-benzyloxycarbonylamino-2-methoxycarbonyl-ethyl)-3-bromo-2-hydroxy-phenoxy]-3,5-dibromo-phenyl}-propionic acid methyl ester 

Relevant articles and documents

Synthetic C6-Functionalized Aminoflavin Catalysts Enable Aerobic Bromination of Oxidation-Prone Substrates

Flavoenzymes catalyze oxidations via hydroperoxide intermediates that result from activation of molecular O2. These reactions—such as hydroxylation and halogenation—depend on the additional catalytic activity of functional groups in the peptide

Synthesis of Isodityrosine, Dityrosine and Related Compounds by Phenolic Oxidation of Tyrosine and Phenylglycine Derivatives Using an Electrochemical Method

The phenolic oxidation of L-tyrosine derivatives by electrolysis and zinc reduction produced the coupling products leading to isodityrosine and dityrosine.The oxidation mode could be controlled by altering halogen substituents (Br or I) at two ortho positions of phenol groups.Additionally, this methodology was applied to 4-hydroxy-D-phenylglycine derivatives, providing the correspoinding oxidative products.