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Molecule
ID:67278
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₀FNO₂
Molecular Mass
183.1796032
Exact Mass
183.06955679
Charge
0
InChI
InChI=1S/C9H10FNO2/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
XWHHYOYVRVGJJY-QMMMGPOBSA-N
Canonic Smiles
N[C@H](C(=O)O)Cc1ccc(cc1)F
Isomeric Smiles
C(=O)([C@@H](N)Cc1ccc(cc1)F)O
Calculated Properties
JChem
Acid pKa
1.8572544
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
-1.0422062
LogD (pH = 7.4)
-1.0457053
Log P
-1.0422492
Molar Refractivity
45.3327
Polarizability
17.601952
Polar Surface Area
63.32
Rotatable Bonds
3
Lipinski's Rule of Five
true
Data Source
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Properties
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Related Proteins
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Molecular Spectra
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Molecule Details
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Bioactivity
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General Information
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IUPAC Traditional name
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Molecular Spectra
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Sigma Aldrich
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
072701
Sigma Aldrich
F4646
47290
Alfa Aesar
L19934
Bide Pharmatech
BD11225
A&J Pharmtech
AJA-O38221
Academic Data
PubChem
716312
Names and Identifiers
IUPAC Traditional name
p-fluorophenylalanine
rac-(2R)-2-amino-3-(4-fluorophenyl)propanoic acid
Synonyms
(S)-4-Fluorophenylalanine
p-Fluoro-L-phenylalanine
4-Fluoro-L-phenylalanine
H-Phe(4-F)-OH
4-Fluoro-L-phenylalanine
4-氟-L-苯基丙氨酸
4-FLUORO-DL-PHENYLALANINE
IUPAC name
(2S)-2-amino-3-(4-fluorophenyl)propanoic acid
rac-(2R)-2-amino-3-(4-fluorophenyl)propanoic acid
Registration numbers
PubChem CID
716312
PubChem SID
162033014
24870843
24278435
MDL Number
MFCD00063064
CAS Number
1132-68-9
51-65-0
Beilstein Number
2416148
Molecule Details
Sigma Aldrich
F4646
Substrates
Substrate for tyrosine hydroxylase that has been used to study the regulation of that enzyme. Substitution of p-fluorophenylalanine for phenylalanine in the culture medium inhibits mitosis and reversibly arrests HeLa cells in G2.
References
PubChem Literature
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Bioactivity
PubChem BioAssay
Registration numbers
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Beilstein Number
Properties
Safety Information
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
3
Source
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
DW1765000
Source
Product Information
95+%
Source
≥99.0% (sum of enantiomers, HPLC)
Source
98%
Source
98+%
Source
C9H10FNO2
Source
puriss.
Source
Pharmacology Properties
human ... TH(7054)mouse ... TH(21823)rat ... TH(25085)
Source
Physical Property
[α]20/D -25±1°, c = 1% in H2O
Source
-25 (c=1 in water)
Source
~255 °C (dec.)
Source
ca 240°C dec.
Source
German water hazard class
Personal Protective Equipment
RTECS
Purity
Empirical Formula (Hill Notation)
Grade
Gene Information
Optical Rotation
Melting Point