135226-82-3

Basic information

• Product Name: 3-acetyl-N,O-dimethyl-N-<(phenylmethoxy)carbonyl>-L-tyrosine methyl ester
• Synonyms: 3-acetyl-N,O-dimethyl-N-<(phenylmethoxy)carbonyl>-L-tyrosine methyl ester
• CAS NO: 135226-82-3
• Molecular Weight: 399.444
• Mol File: 135226-82-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-acetyl-N,O-dimethyl-N-<(phenylmethoxy)carbonyl>-L-tyrosine methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-acetyl-N,O-dimethyl-N-<(phenylmethoxy)carbonyl>-L-tyrosine methyl ester(135226-82-3)
• EPA Substance Registry System: 3-acetyl-N,O-dimethyl-N-<(phenylmethoxy)carbonyl>-L-tyrosine methyl ester(135226-82-3)

Safety Data

• Hazardous Substances Data: 135226-82-3(Hazardous Substances Data)

Upstream product

• 110774-03-3 L-3-(3-acetyl-4-hydroxyphenyl)-N-(benzyloxycarbonyl)alanine methyl ester 
• 74-88-4 methyl iodide 

Downstream Products

• 109011-07-6 C₄₁H₅₂N₆O₁₀ 
• 135226-88-9 (S)-2-{[(S)-2-(Benzyloxycarbonyl-methyl-amino)-3-(4-iodo-phenyl)-propionyl]-methyl-amino}-3-(3-hydroxy-4-methoxy-phenyl)-propionic acid methyl ester 
• 135226-90-3 BOC-D-alanyl-L-alanyl-N,O-dimethyl-L-tyrosyl-L-alanyl-N-methyl-L-tyrosyl-N,O-dimethyl-L-tyrosine cyclic 5⁴<*>6³ ether, methyl ester 
• 135226-91-4 C₄₆H₆₀N₆O₁₂ 
• 122621-60-7 RA-VII 
• 64725-24-2 deoxybouvadin 
• 135226-89-0 methyl 4-methoxy-12-amino>-N¹⁰-methyl-11-oxo-2-azatricyclo<12.2.2.1^3,7>nonadeca-3,5,7(19),14,16,17-hexaene-9-carboxylate 
• 135226-84-5 3-hydroxy-N,O-dimethyl-N-<(phenylmethoxy)carbonyl>-L-tyrosine methyl ester 
• 135226-85-6 N,O⁴-dimethyl-L-DOPA methyl ester 
• 135226-83-4 (S)-3-(3-Acetoxy-4-methoxy-phenyl)-2-(benzyloxycarbonyl-methyl-amino)-propionic acid methyl ester 

Relevant articles and documents

Synthesis of new DOPA derivative from l-tyrosine for construction of bioactive compound

A practical synthetic method of new DOPA derivative was developed with L-tyrosine as starting material. The new DOPA analogue could be used in building bioactive compounds.

Total synthesis of deoxybouvardin and RA-VII: Macrocyclization via an intramolecular Ullmann reaction

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