ChemicalBook > Product Catalog > Biochemical Engineering > Amino Acids and Derivatives > BOC-amino acid > (S)-3-(Boc-amino)-4-phenylbutyric acid
(S)-3-(Boc-amino)-4-phenylbutyric acid
(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
- Product Categories:
-
- Benzotriazoles ,Triazoles
- Amino Acid Derivatives
- β-Homo Amino Acids
- Beta amino acids
- Mol File:
- 51871-62-6.mol
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(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
- form
- powder to crystal
- pka
- 4.43±0.10(Predicted)
- color
- White to Almost white
- optical activity
- [α]20/D 19.0±2°, c = 1% in methylene chloride
- BRN
- 3060457
- Major Application
- peptide synthesis
- InChI
- 1S/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
- InChIKey
- ACKWQHCPHJQANL-LBPRGKRZSA-N
- SMILES
- CC(C)(C)OC(=O)N[C@H](CC(O)=O)Cc1ccccc1
- CAS DataBase Reference
- 51871-62-6(CAS DataBase Reference)
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Safety Information
- Safety Statements
- 24/25
- WGK Germany
- 3
- HazardClass
- IRRITANT
- HS Code
- 29242990
- Storage Class
- 11 - Combustible Solids
MSDS
- Language:English Provider:SigmaAldrich
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(S)-3-(Boc-amino)-4-phenylbutyric acid Usage And Synthesis
Chemical Properties
White to off-white powder
Uses
peptide synthesis
reaction suitability
reaction 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.
(S)-3-(Boc-amino)-4-phenylbutyric acidSupplier
Shanghai HC Biotech Co., Ltd
- Tel
- 021-20227858
- sale@hcbiotech.com.cn
INTATRADE GmbH
- Tel
- +49 3493/605464
- sales@intatrade.de
3B Pharmachem (Wuhan) International Co.,Ltd.
- Tel
- 821-50328103-801 18930552037
- 3bsc@sina.com
Alfa Aesar
- Tel
- 400-6106006
- saleschina@alfa-asia.com
Energy Chemical
- Tel
- 021-021-58432009 400-005-6266
- sales8178@energy-chemical.com
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(S)-3-(Boc-amino)-4-phenylbutyric acid(51871-62-6)Related Product Information
- 6-Aminocaproic acid
- Indole-3-butyric acid
- 4-Aminobutyric acid
- 4-Phenylbutyric acid
- Glycine
- BOC-(S)-3-AMINO-4-(3-FLUOROPHENYL)BUTYRIC ACID
- BOC-(S)-3-AMINO-4-(4-NITRO-PHENYL)-BUTYRIC ACID
- BOC-(S)-3-AMINO-4-(3-METHYL-PHENYL)-BUTYRIC ACID
- BOC-(S)-3-AMINO-4-(1-NAPHTHYL)-BUTYRIC ACID
- BOC-(S)-3-AMINO-4-(4-BROMO-PHENYL)-BUTYRIC ACID
- BOC-(S)-2-TETRAHYDROISOQUINOLINE ACETIC ACID
- BOC-(S)-3-AMINO-4-(2-CHLORO-PHENYL)-BUTYRIC ACID
- BOC-(S)-3-AMINO-4-(4-FLUORO-PHENYL)-BUTYRIC ACID
- BOC-(S)-3-AMINO-4-(2,4-DICHLORO-PHENYL)-BUTYRIC ACID
- BOC-(S)-3-AMINO-4-(2-METHYL-PHENYL)-BUTYRIC ACID
- BOC-(S)-3-AMINO-4-(2-NAPHTHYL)-BUTYRIC ACID
- BOC-(S)-3-AMINO-4-(3-CHLORO-PHENYL)-BUTYRIC ACID
- BOC-(S)-3-AMINO-4-(4-CHLORO-PHENYL)-BUTYRIC ACID