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(S)-3-(Boc-amino)-4-phenylbutyric acid

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Company Name: Shanghai HC Biotech Co., Ltd  
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(S)-3-(Boc-amino)-4-phenylbutyric acid manufacturers
(S)-3-(Boc-amino)-4-phenylbutyric acid Basic information
Product Name:(S)-3-(Boc-amino)-4-phenylbutyric acid
Synonyms:N-beta-(t-Butyloxycarbonyl)-L-Homophenylalanine;-Homophe-OH;(S)-b-(Boc-amino)benzenebutanoic acid;Boc-beta-Homophe-OH >=98.0% (TLC);(S)-Boc-3-amino-4-phenylbutyric acid;(S)-3-(tert-Butyloxycarbonyl)amino-4-phenylbutyric acid;(S)-3-(BOC-AMINO)-4-PHENYLBUTYRIC ACID;(S)-BOC-B2-HOPHE-OH
CAS:51871-62-6
MF:C15H21NO4
MW:279.33
EINECS:
Product Categories:Benzotriazoles ,Triazoles;Amino Acid Derivatives;β-Homo Amino Acids;Beta amino acids
Mol File:51871-62-6.mol
(S)-3-(Boc-amino)-4-phenylbutyric acid Structure
(S)-3-(Boc-amino)-4-phenylbutyric acid Chemical Properties
Melting point 101-107 °C
Boiling point 444.8±38.0 °C(Predicted)
density 1.139
storage temp. Sealed in dry,Room Temperature
solubility soluble in Methanol
pka4.43±0.10(Predicted)
form powder to crystal
color White to Almost white
Optical Rotation[α]20/D 19.0±2°, c = 1% in methylene chloride
BRN 3060457
Major Applicationpeptide synthesis
InChI1S/C15H21NO4/c1-15(2,3)20-14(19)16-12(10-13(17)18)9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,16,19)(H,17,18)/t12-/m0/s1
InChIKeyACKWQHCPHJQANL-LBPRGKRZSA-N
SMILESCC(C)(C)OC(=O)N[C@H](CC(O)=O)Cc1ccccc1
CAS DataBase Reference51871-62-6(CAS DataBase Reference)
Safety Information
Safety Statements 24/25
WGK Germany 3
HazardClass IRRITANT
HS Code 29242990
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
(S)-3-(Boc-amino)-4-phenylbutyric acid Usage And Synthesis
Chemical PropertiesWhite to off-white powder
Usespeptide synthesis
reaction suitabilityreaction type: Boc solid-phase peptide synthesis
Synthesis

Chiral (S)-3-(Boc-amino)-4-phenylbutyric acid is a carboxylic organic compound, and it has been reported in the literature that chiral N-Boc-3-arylmethyl-5-oxoisoxazoles can be synthesized in a one-pot synthesis by a sequential reaction such as cross-complex decomposition reaction, asymmetric conjugate addition reaction, and oxidative reaction using allyl aromatic compounds with crotonaldehyde as starting materials.

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