4-Fluoro-Phe-OH
Suppliers
Names
[ CAS No. ]:
1132-68-9
[ Name ]:
4-Fluoro-Phe-OH
[Synonym ]:
L-4-FLUOROPHE
(2R)-2-Amino-3-(4-fluorophenyl)propanoic acid
D,L-p-fluorophenylalanine
L-4-F-Phe-OH
L-p-fluorophenylalanine
4-Fluorophenylalanine
H-Phe(4-F)-OH
H-L-PHE(4-F)-OH
L-4-Fluorophenylalanine
4-fluoroPhe
RARECHEM BK PT 0031
(2R)-2-amino-3-(4-fluorophenyl)propionic acid
D-4-Fluorophenylalanine
Phenylalanine, 4-fluoro-
para-fluoro-l-phenylalanine
H-PHE(P-F)-OH
D-4-Fluorophe
H-P-FLUORO-PHE-OH
(S)-2-Amino-3-(4-fluorophenyl)propanoic acid
4-Fluoro-Phe-OH
MFCD00063064
S-(-)-p-Fluorophenylalanine
para-fluorophenylalanine
p-Fluoro-L-phenylalanine
L-4-Fluoro-Phenylalanine
D,L-4-fluorophenylalanine
L-4-Fluoro-phe-OH
(2S)-2-amino-3-(4-fluorophenyl)propanoic acid
H-D-Phe(4-F)-OH
(S)-4-Fluorophenylalanine
4-Fluoro-L-phenylalanine
(S)-2-Amino-3-(4-fluorophenyl)propionic Acid
4-FLUOROPHENYLALANINE, D-
Chemical & Physical Properties
[ Density]:
1.3±0.1 g/cm3
[ Boiling Point ]:
313.3±32.0 °C at 760 mmHg
[ Melting Point ]:
~255 °C (dec.)
[ Molecular Formula ]:
C9H10FNO2
[ Molecular Weight ]:
183.180
[ Flash Point ]:
143.3±25.1 °C
[ Exact Mass ]:
183.069550
[ PSA ]:
63.32000
[ LogP ]:
1.16
[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C
[ Index of Refraction ]:
1.555
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
[ Hazard Codes ]:
Xi
[ Safety Phrases ]:
S23-S24/25
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ RTECS ]:
DW1765000
Synthetic Route
Precursor & DownStream
Precursor
DownStream
Articles
Nat. Chem. Biol. 3(5) , 268-273, (2007)
The identification of self-renewing and multipotent neural stem cells (NSCs) in the mammalian brain holds promise for the treatment of neurological diseases and has yielded new insight into brain canc...
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Studies of gene function and molecular mechanisms in Plasmodium falciparum are hampered by difficulties in characterizing and measuring phenotypic differences between individual parasites. We screened...
J. Biol. Chem. 269 , 24637, (1994)
Tetrahydropterins react with phenylalanine hydroxylase at a redox site, a regulatory site, and the catalytic site, but neither the properties of nor relationships among these sites are well understood...