866114-96-7

Basic information

• Product Name: (S)-4-(3-(Benzyloxy)-2-(benzyloxycarbonylamino)-3-oxopropyl)phenylboronic acid
• Synonyms: (S)-4-(2-(Benzyloxycarbonyl)-2-(Cbz-amino)ethyl)phenylboronic acid;(S)-4-(3-(Benzyloxy)-2-(benzyloxycarbonylamino)-3-oxopropyl)phenylboronic acid
• CAS NO: 866114-96-7
• Molecular Formula: C₂₄H₂₄BNO₆
• Molecular Weight: 433.26146
• Mol File: 866114-96-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Density: 1.28±0.1 g/cm3(Predicted)
• Storage Temp.: Room temperature.
• PKA: 8.56±0.16(Predicted)
• CAS DataBase Reference: (S)-4-(3-(Benzyloxy)-2-(benzyloxycarbonylamino)-3-oxopropyl)phenylboronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-4-(3-(Benzyloxy)-2-(benzyloxycarbonylamino)-3-oxopropyl)phenylboronic acid(866114-96-7)
• EPA Substance Registry System: (S)-4-(3-(Benzyloxy)-2-(benzyloxycarbonylamino)-3-oxopropyl)phenylboronic acid(866114-96-7)

Safety Data

• Hazardous Substances Data: 866114-96-7(Hazardous Substances Data)

Usage

General Description

"(S)-4-(3-(Benzyloxy)-2-(benzyloxycarbonylamino)-3-oxopropyl)phenylboronic acid" is a complex organic compound that consists of several functional groups. It belongs to the class of chemical compounds known as boronic acids, which contain a boron atom bonded to an oxygen atom and two carbon atoms. The "S-" in its name indicates the stereochemistry i.e., the spatial arrangement of atoms. (S)-4-(3-(Benzyloxy)-2-(benzyloxycarbonylamino)-3-oxopropyl)phenylboronic acid features a benzyloxy group (a benzyl group bound to an oxygen atom) and a carboxyl group (COOH) carrying an additional benzyl group), indicating potential applications in organic synthesis due to their tendency to undergo a variety of chemical reactions. The specific properties, toxicity, and practical uses of this particular compound could vary and would typically need to be evaluated individually.

Upstream product

• 214491-30-2 N-benzyloxycarbonyl-4-(2,3-dimethyl-2,3-butanediolatoboryl)-L-phenylalanine benzyl ester 
• 866115-03-9 (S)-2-Benzyloxycarbonylamino-3-[4-(5,5-dimethyl-[1,3,2]dioxaborinan-2-yl)-phenyl]-propionic acid benzyl ester 
• 1991-81-7 4-iodo-L-phenylalanine 
• 501-53-1 benzyl chloroformate 
• 220400-04-4 N-<(Benzyloxy)carbonyl>-4-iodo-L-phenylalanine 
• 257628-00-5 N-benzyloxycarbonyl-4-iodo-L-phenylalanine benzyl ester 
• 5513-40-6 benzyl N-carbobenzyloxy-L-tyrosine 
• 100-39-0 benzyl bromide 
• 183070-41-9 L-N^α-Cbz-4-(O-trifluoromethanesulfonate)tyrosine benzyl ester 
• 262603-98-5 Cbz-Tyr(Nf)-OBzl 

Downstream Products

• 866115-05-1 (S)-2-Benzyloxycarbonylamino-3-{3-[4-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-phenoxy]-4-hydroxy-phenyl}-propionic acid benzyl ester 
• 866115-06-2 (S)-2-Benzyloxycarbonylamino-3-{3-[4-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-phenoxy]-5-bromo-4-hydroxy-phenyl}-propionic acid benzyl ester 
• 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 
• 76410-58-7 p-borono-L-phenylalanine 
• 866115-04-0 (S)-2-Benzyloxycarbonylamino-3-[3-[4-((S)-2-benzyloxycarbonyl-2-benzyloxycarbonylamino-ethyl)-phenoxy]-4-(4-methoxy-benzyloxy)-phenyl]-propionic acid benzyl ester 
• 164203-33-2 N-benzyloxycarbonyl-4-borono-L-phenylalanine 

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