| Identification | More | [Name]
Boc-L-homophenylalanine | [CAS]
100564-78-1 | [Synonyms]
2-tert-Butoxycarbonylamino-4-(S)-phenylbutyric acid
BOC-(+)-ALPHA-AMINO-4-PHENYLBUTYRIC ACID
BOC-HFE-OH
BOC-HOMO-L-PHENYLALANINE
BOC-HOMOPHENYLALANINE
BOC-HOMOPHE-OH
BOC-HOPHE-OH
BOC-HPH-OH
BOC-L-HOMOPHE
BOC-L-HOMOPHENYL-ALA
BOC-L-HOMOPHENYLALANINE
BOC-L-HOPHE-OH
BOC-L-HPH
BOC-L-HPHE
Boc-L-HPhe-OH
BOC-(S)-2-AMINO-4-PHENYLBUTYRIC ACID
N-ALPHA-BUTOXYCARBONYL-(+)-ALPHA-AMINO-4-PHENYLBUTYRIC ACID
N-ALPHA-T-BOC-L-HOMOPHENYLALANINE
N-ALPHA-TERT-BUTYLOXYCARBONYL-L-HOMO-PHENYLALANINE
N-BOC-(L)-HOMOPHENYLALANINE | [Molecular Formula]
C15H21NO4 | [MDL Number]
MFCD00076904 | [Molecular Weight]
279.33 | [MOL File]
100564-78-1.mol |
| Chemical Properties | Back Directory | [Melting point ]
76-80 °C | [Boiling point ]
439.6±38.0 °C(Predicted) | [density ]
1.139 | [storage temp. ]
2-8°C
| [solubility ]
Soluble in methanol. | [form ]
powder to crystal | [pka]
3.95±0.10(Predicted) | [color ]
White to Almost white | [Optical Rotation]
[α]20/D +6.5±1°, c = 2% in ethanol | [BRN ]
3653506 | [Major Application]
peptide synthesis | [InChI]
InChI=1/C15H21NO4/c1-15(2,3)20-14(19)16-12(13(17)18)10-9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,16,19)(H,17,18)/t12-/s3 | [InChIKey]
MCODLPJUFHPVQP-LBPRGKRZSA-N | [SMILES]
[C@@H](C(=O)O)(CCC1=CC=CC=C1)NC(=O)OC(C)(C)C |&1:0,r| | [CAS DataBase Reference]
100564-78-1(CAS DataBase Reference) |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H302-H315-H319-H335 | [Precautionary statements ]
P261-P301+P312-P302+P352-P304+P340-P305+P351+P338 | [Hazard Codes ]
Xi | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [F ]
3-10 | [HazardClass ]
IRRITANT | [HS Code ]
29242990 | [Storage Class]
11 - Combustible Solids |
| Hazard Information | Back Directory | [Chemical Properties]
White powder | [Uses]
N-Boc-L-homophenylalanine is a useful reagent for organic synthesis and other chemical processes. It is used in the preparation of piperidine-containing peptidyl proteasome inhibitors. | [reaction suitability]
reaction type: Boc solid-phase peptide synthesis |
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