600737-82-4

Basic information

• Product Name: L-Tyrosine, N-[(phenylmethoxy)carbonyl]-O-(phenylmethyl)-3-(4,4,5,5-tetramethyl-1, 3,2-dioxaborolan-2-yl)-, phenylmethyl ester
• CAS NO: 600737-82-4
• Molecular Formula: C37H40BNO7
• Molecular Weight: 621.538
• Mol File: 600737-82-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: L-Tyrosine, N-[(phenylmethoxy)carbonyl]-O-(phenylmethyl)-3-(4,4,5,5-tetramethyl-1, 3,2-dioxaborolan-2-yl)-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Tyrosine, N-[(phenylmethoxy)carbonyl]-O-(phenylmethyl)-3-(4,4,5,5-tetramethyl-1, 3,2-dioxaborolan-2-yl)-, phenylmethyl ester(600737-82-4)
• EPA Substance Registry System: L-Tyrosine, N-[(phenylmethoxy)carbonyl]-O-(phenylmethyl)-3-(4,4,5,5-tetramethyl-1, 3,2-dioxaborolan-2-yl)-, phenylmethyl ester(600737-82-4)

Safety Data

• Hazardous Substances Data: 600737-82-4(Hazardous Substances Data)

Usage

Description

L-Tyrosine, N-[(phenylmethoxy)carbonyl]-O-(phenylmethyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, phenylmethyl ester is a complex organic compound derived from L-Tyrosine, a non-essential amino acid. It features a phenylmethoxycarbonyl group, a phenylmethyl group, and a tetramethyl-1,3,2-dioxaborolan-2-yl moiety attached to its structure. L-Tyrosine,
N-[(phenylmethoxy)carbonyl]-O-(phenylmethyl)-3-(4,4,5,5-tetramethyl-1,
3,2-dioxaborolan-2-yl)-, phenylmethyl ester is characterized by its unique chemical properties and potential applications in various fields.

Uses

Used in Pharmaceutical Industry:
L-Tyrosine, N-[(phenylmethoxy)carbonyl]-O-(phenylmethyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, phenylmethyl ester is used as an intermediate in the preparation of L,L-Dityrosine Dihydrochloride (D494290), a compound with potential pharmaceutical applications.
Used in Chemical Synthesis:
L-Tyrosine,
N-[(phenylmethoxy)carbonyl]-O-(phenylmethyl)-3-(4,4,5,5-tetramethyl-1,
3,2-dioxaborolan-2-yl)-, phenylmethyl ester can also be used as a building block in the synthesis of various organic compounds, particularly those involving the formation of new carbon-carbon or carbon-heteroatom bonds. Its unique structure allows for versatile synthetic applications in organic chemistry.

Upstream product

• 213757-66-5 (S)-2-Benzyloxycarbonylamino-3-(4-hydroxy-3-iodo-phenyl)-propionic acid benzyl ester 
• 501-53-1 benzyl chloroformate 
• 100-39-0 benzyl bromide 
• 5513-40-6 benzyl N-carbobenzyloxy-L-tyrosine 
• 70-78-0 3-Iodo-L-tyrosine 
• 73183-34-3 bis(pinacol)diborane 
• 600737-79-9 benzyl (S)-3-(4-(benzyloxy)-3-iodophenyl)-2-(((benzyloxy)carbonyl)amino)propanoate 
• 79677-62-6 (S)-2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxy-3-iodophenyl)propanoic acid 
• 315203-50-0 N-benzyloxycarbonyl-O-benzyl-L-tyrosine benzyl ester 

Downstream Products

• 866115-07-3 (S)-3-{2'-Benzyloxy-5'-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-5-[4-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-phenoxy]-6-hydroxy-biphenyl-3-yl}-2-benzyloxycarbonylamino-propionic acid benzyl ester 
• 600737-85-7 (S)-2-Benzyloxycarbonylamino-3-[6,2'-bis-benzyloxy-5'-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-biphenyl-3-yl]-propionic acid benzyl ester 

Relevant articles and documents

Synthesis of the side chain cross-linked tyrosine oligomers dityrosine, trityrosine, and pulcherosine

An efficient synthesis of dityrosine and the first syntheses of the tyrosine trimers trityrosine and pulcherosine have been achieved. Protected 3-iodotyrosine underwent tandem Miyaura borylation-Suzuki coupling to give protected dityrosine. The choice of