| Identification | More | [Name]
BOC-L-4,4'-BIPHENYLALANINE | [CAS]
147923-08-8 | [Synonyms]
3-(4-BIPHENYLYL)-N-(T-BUTOXYCARBONYL)-L-ALANINE
3-(4-BIPHENYLYL)-N-(TERT-BUTOXYCARBONYL)-L-ALANINE
3-(BIPHENYL-4-YL)-N-TERT-BUTYROXYCARBONYL-ALANINE
BOC-3-(4-BIPHENYLYL)-L-ALANINE
BOC-4-BIPHENYL-L-ALA
BOC-4-PHENYL-L-PHENYLALANINE
BOC-4-PHENYL-PHENYLALANINE
BOC-4-PHENYL-PHE-OH
BOC-BETA-(4-BIPHENYLYL)-ALA-OH
BOC-BIP(4,4')-OH
BOC-BIP-OH
BOC-BPH-OH
BOC-L-4,4'-BIPHENYLALANINE
BOC-L-ALA(4,4'-BIPHENYL)-OH
BOC-L-BIPHENYLALANINE
BOC-L-BIP-OH
BOC-L-PHE(4-PH)
BOC-PHE(4-PHENYL)-OH
BOC-P-PHENYL-L-PHE-OH
BOC-(S)-2-AMINO-3-(1,1'-BIPHENY-4-YL)PROPANOIC ACID | [Molecular Formula]
C20H23NO4 | [MDL Number]
MFCD00191184 | [Molecular Weight]
341.4 | [MOL File]
147923-08-8.mol |
| Chemical Properties | Back Directory | [Melting point ]
103-107 °C(lit.) | [Boiling point ]
528.2±50.0 °C(Predicted) | [density ]
1.161±0.06 g/cm3(Predicted) | [storage temp. ]
Store at RT. | [solubility ]
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
3.88±0.10(Predicted) | [color ]
White to Off-White | [optical activity]
[α]22/D +21°, c = 2 in methanol | [CAS DataBase Reference]
147923-08-8(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
N,Xi,Xn | [Risk Statements ]
R50/53:Very Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment .
R41:Risk of serious damage to eyes.
R38:Irritating to the skin.
R20/22:Harmful by inhalation and if swallowed . | [Safety Statements ]
S60:This material and/or its container must be disposed of as hazardous waste .
S61:Avoid release to the environment. Refer to special instructions safety data sheet .
S36:Wear suitable protective clothing .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [RIDADR ]
UN 3077 9/PG 3
| [WGK Germany ]
3
| [HS Code ]
29242990 |
| Hazard Information | Back Directory | [Chemical Properties]
White powder | [Uses]
N-Boc-4-phenyl-L-phenylalanine is a reactant used in the synthesis of novel phenylalanines derived diamides as factor XIa inhibitors used in the treatment. | [reaction suitability]
reaction type: Boc solid-phase peptide synthesis |
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