| Identification | More | [Name]
(S)-3-(Boc-amino)-4-phenylbutyric acid | [CAS]
51871-62-6 | [Synonyms]
BOC-BETA-HOMOPHENYLALANINE
BOC-BETA-HOMOPHE-OH
BOC-BETA-HOPHE-OH
BOC-BETA-HPH-OH
BOC-HOMOPHE(BETA)-OH
BOC-L-BETA-HOMOPHENYLALANINE
BOC-PHE-(C*CH2)OH
N-BETA-T-BUTOXYCARBONYL-L-BETA-HOMOPHENYLALANINE
N-T-BUTOXYCARBONYL-(S)-3-AMINO-4-PHENYLBUTYRIC ACID
(S)-3-(BOC-AMINO)-4-PHENYLBUTYRIC ACID
(S)-3-(tert-Butyloxycarbonyl)amino-4-phenylbutyric acid
(S)-BOC-B2-HOPHE-OH
(S)-BOC-BETA2-HOMOPHENYLALANINE
(S)-BOC-BETA2-HPH-OH
Boc-(S)-3-Amino-4-phenylpropionic acid
Boc-L-b-homophenylalanine
Boc-L-β-Homo-Phe-OH
Boc-L-β-homophenylalanine, HPLC 98%
BOC-SS-HOMOPHE
Boc-L-beta-HPhe-OH | [Molecular Formula]
C15H21NO4 | [MDL Number]
MFCD01076271 | [Molecular Weight]
279.33 | [MOL File]
51871-62-6.mol |
| Chemical Properties | Back Directory | [Melting point ]
101-107 °C | [Boiling point ]
444.8±38.0 °C(Predicted) | [density ]
1.139 | [storage temp. ]
Store at?0-5°C | [solubility ]
soluble in Methanol | [form ]
powder to crystal | [pka]
4.43±0.10(Predicted) | [color ]
White to Almost white | [Optical Rotation]
[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) |
| Hazard Information | Back Directory | [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-c |
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