90819-30-0

Basic information

• Product Name: (S)-2-TERT-BUTOXYCARBONYLAMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID
• Synonyms: 2(S)-TERT-BUTOXYCARBONYLAMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID;BOC-3-HYDROXY-L-PHENYLALANINE;BOC-M-TYR-OH;BOC-L-META-TYROSINE;BOC-L-PHE(3-OH)-OH;BOC-L-M-TYR;(S)-2-TERT-BUTOXYCARBONYLAMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID;N-Boc-3-hydroxy-L-phenylalanine
• CAS NO: 90819-30-0
• Molecular Formula: C₁₄H₁₉NO₅
• Molecular Weight: 281.3
• Mol File: 90819-30-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: Store at 0-5°C
• CAS DataBase Reference: (S)-2-TERT-BUTOXYCARBONYLAMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-TERT-BUTOXYCARBONYLAMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID(90819-30-0)
• EPA Substance Registry System: (S)-2-TERT-BUTOXYCARBONYLAMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID(90819-30-0)

Safety Data

• Hazardous Substances Data: 90819-30-0(Hazardous Substances Data)

Usage

General Description

"(S)-2-TERT-BUTOXYCARBONYLAMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID" is a chemical compound that belongs to the class of amino acids. It is a derivative of the amino acid phenylalanine, with a tert-butoxycarbonyl (Boc) protecting group attached to the amino group. (S)-2-TERT-BUTOXYCARBONYLAMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID has potential applications in peptide synthesis and drug development due to its ability to modify and protect the structure of amino acids. It is also known for its anti-inflammatory properties, making it a potential candidate for the development of anti-inflammatory drugs. The (S)-2-TERT-BUTOXYCARBONYLAMINO-3-(3-HYDROXY-PHENYL)-PROPIONIC ACID is a valuable compound with diverse applications in the field of chemistry and pharmacology.

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 587-33-7 m-tyrosine 
• 775-06-4 D/L-3-hydroxy-phenylalanine 
• 58632-95-4 2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile 

Downstream Products

• 1175919-93-3 C₁₇H₂₃NO₅ 
• 1415657-97-4 tert-butyl ((S)-3-(3-hydroxyphenyl)-1-((S)-3-(((3-iodobenzyl)oxy)-methyl)-3,4-dihydroisoquinolin-2(1H)-yl)-1-oxopropan-2-yl)-carbamate 
• 1415657-94-1 tert-butyl ((S)-3-(3-hydroxyphenyl)-1-(((1S,2R)-1-((3-iodobenzyl)-oxy)-1-phenylpropan-2-yl)(methyl)amino)-1-oxopropan-2-yl)-carbamate 
• 1381817-13-5 C₄₅H₆₆N₄O₉Si 
• 1381814-74-9 (S)-1-{(S)-2-tert-butoxycarbonylamino-3-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-propionyl}-hexahydro-pyridazine-3-carboxylic acid 2,2,2-trichloro-ethyl ester 
• 1381809-66-0 (13E,15E)-(3S,6S,9R,10R,11S,12S,21S)-3-(3-hydroxy-benzyl)-10,12-dimethoxy-6-(4-methoxy-benzyl)-9,11-dimethyl-19-oxa-1,4,7,25-tetraazabicyclo[19.3.1]pentacosa-13,15-diene-2,5,8,20-tetraone 
• 162538-23-0 [(S)-1-(3-Benzyloxy-benzyl)-3-((S)-3-tert-butoxycarbonylamino-2-hydroxy-4-phenyl-butylamino)-2-hydroxy-propyl]-carbamic acid tert-butyl ester 

Relevant articles and documents

Elucidating the Structural Requirement of Uridylpeptide Antibiotics for Antibacterial Activity

The synthesis and biological evaluation of analogues of uridylpeptide antibiotics were described, and the molecular interaction between the 3′-hydroxy analogue of mureidomycin A (3′-hydroxymureidomycin A) and its target enzyme, phospho-MurNAc-pentapeptide

Synthesis of [L-m-Tyr1]- and [D-m-Tyr1]-leucine-enkephalin via the REMA method

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