| Identification | More | [Name]
4-Bromo-L-phenylalanine | [CAS]
24250-84-8 | [Synonyms]
3-(4-BROMOPHENYL)-L-ALANINE
4-BROMO-L-PHENYLALANINE
4-BROMO-L-PHENYLALANINE HYDROCHLORIDE
4-BROMO-L-PHE-OH
4-BROMO-L-PHE-OH HCL
H-L-PHE(4-BR)-OH
H-P-BROMO-L-PHE-OH
H-P-BROMO-PHE-OH
H-PHE(4-BR)-OH
H-PHE(P-BR)-OH
L-4-BROMOPHE
L-4-BROMOPHENYLALANINE
L-4-BR-PHE
L-P-BROMOPHENYLALANINE
L-PHE(4-BR)
P-BROMO-L-PHENYLALANINE
P-BROMO-PHENYLALANINE
RARECHEM BK PT 0043
(S)-2-AMINO-3-(4-BROMO-PHENYL)-PROPIONIC ACID
(S)-2-Amino-3-(4'-Bromophenyl)Propanoic Acid | [Molecular Formula]
C9H10BrNO2 | [MDL Number]
MFCD00063062 | [Molecular Weight]
244.09 | [MOL File]
24250-84-8.mol |
| Chemical Properties | Back Directory | [Melting point ]
~265 °C (dec.)
| [Boiling point ]
368.4±32.0 °C(Predicted) | [density ]
1.588±0.06 g/cm3(Predicted) | [storage temp. ]
Store at RT. | [solubility ]
Methanol (Slightly, Sonicated), Water (Slightly, Heated, Sonicated) | [form ]
Solid | [pka]
2.18±0.10(Predicted) | [color ]
White to Off-White | [Optical Rotation]
[α]20/D 22.0±2°, c = 0.5% in H2O | [BRN ]
2212159 | [Stability:]
Hygroscopic | [Major Application]
peptide synthesis | [InChI]
InChI=1S/C9H10BrNO2/c10-7-3-1-6(2-4-7)5-8(11)9(12)13/h1-4,8H,5,11H2,(H,12,13)/t8-/m0/s1 | [InChIKey]
PEMUHKUIQHFMTH-QMMMGPOBSA-N | [SMILES]
C(O)(=O)[C@H](CC1=CC=C(Br)C=C1)N | [CAS DataBase Reference]
24250-84-8(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
T,Xi | [Risk Statements ]
R25:Toxic if swallowed. | [Safety Statements ]
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [RIDADR ]
UN2811 | [WGK Germany ]
3
| [HazardClass ]
6.1 | [PackingGroup ]
III | [HS Code ]
2922498590 | [Storage Class]
6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects | [Hazard Classifications]
Acute Tox. 3 Oral |
| Hazard Information | Back Directory | [Chemical Properties]
Off-white powder | [Uses]
peptide synthesis | [reaction suitability]
reaction type: solution phase peptide synthesis | [Synthesis]
A solution of compound (S)-acetyl-protected raw material (10 g, 0.048 mol) in 10% aqueous hydrochloric acid (100 mL) was stirred at 95-100 °C for 6 h and then the pH was neutralized with triethylamine. The solid was collected by filtration and washed with |
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