160538-43-2

Basic information

• Product Name: (R)-Benzyloxycarbonylamino-(4-hydroxy-3,5-diiodo-phenyl)-acetic acid methyl ester
• CAS NO: 160538-43-2
• Molecular Weight: 567.119
• Mol File: 160538-43-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-Benzyloxycarbonylamino-(4-hydroxy-3,5-diiodo-phenyl)-acetic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-Benzyloxycarbonylamino-(4-hydroxy-3,5-diiodo-phenyl)-acetic acid methyl ester(160538-43-2)
• EPA Substance Registry System: (R)-Benzyloxycarbonylamino-(4-hydroxy-3,5-diiodo-phenyl)-acetic acid methyl ester(160538-43-2)

Safety Data

• Hazardous Substances Data: 160538-43-2(Hazardous Substances Data)

Upstream product

• 26531-82-8 (S)-methyl 2-amino-2-(4-hydroxyphenyl)acetate 
• 32462-30-9 (S)-hydroxyphenylglycine 
• 213136-30-2 (R)-2-(((benzyloxy)carbonyl)amino)-2-(4-hydroxyphenyl)acetate methyl ester 

Relevant articles and documents

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.