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Molecule
ID:97192
Structure
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Functional Group
Text
General Information
Structure
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Molecular Formula
C₉H₁₀FNO₂
Molecular Mass
183.1796032
Exact Mass
183.06955679
Charge
0
InChI
InChI=1S/C9H10FNO2/c10-7-3-1-2-6(4-7)5-8(11)9(12)13/h1-4,8H,5,11H2,(H,12,13)
InChIKey
VWHRYODZTDMVSS-UHFFFAOYSA-N
Canonic Smiles
OC(=O)C(Cc1cccc(c1)F)N
Isomeric Smiles
NC(Cc1cccc(c1)F)C(=O)O
Calculated Properties
JChem
Acid pKa
1.8590033
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
-1.0421922
LogD (pH = 7.4)
-1.046044
Log P
-1.0422448
Molar Refractivity
45.3327
Polarizability
17.601942
Polar Surface Area
63.32
Rotatable Bonds
3
Lipinski's Rule of Five
true
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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 name
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IUPAC Traditional name
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Physical Property
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Molecular Spectra
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MP Biomedicals
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Alfa Aesar
L07297
Apollo Scientific
PC4148
MP Biomedicals
02101706
05214621
Sigma Aldrich
F5126
219436
47310
Academic Data
PubChem
9976
Names and Identifiers
Synonyms
3-Fluoro-DL-phenylalanine
H-DL-Phe(3-F)-OH
3-氟-DL-苯基丙胺酸
3-Fluoro-DL-phenylalanine 98%
3-Fluoro-DL-phenylalanine
m-FLUORO-DL-PHENYLALANINE
DL-β-m-FLUOROPHENYLALANINE
3-氟-DL-苯丙氨酸
m-Fluoro-DL-phenylalanine
IUPAC name
2-amino-3-(3-fluorophenyl)propanoic acid
IUPAC Traditional name
3-fluorophenylalanine
Registration numbers
CAS Number
2629-54-1
456-88-2
MDL Number
MFCD00004273
EC Number
220-104-1
Beilstein Number
2939807
PubChem SID
24894882
162083804
24870870
PubChem CID
9976
Molecule Details
MP Biomedicals
02101706
Inhibitor of protein synthesis; phenylalanine antagonist.
Crystalline
05214621
MP Biomedicals Rare Chemical collection
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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CAS Number
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MDL Number
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EC Number
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Beilstein Number
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PubChem SID
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PubChem CID
Properties
Physical Property
Melting Point
240-250°C
Source
~240 °C (dec.)
Source
ca 245°C dec.
Source
Safety Information
Storage Warning
Harmful
Source
Storage Condition
Room Temperature (15-30°C)
Source
MSDS Link
Download link
Source
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European Hazard Symbols
Irritant (Xi)
Source
German water hazard class
3
Source
Safety Statements
24/25
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
Risk Statements
37
Source
TSCA Listed
否
Source
Product Information
Certificate of Analysis
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Source
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Linear Formula
FC6H4CH2CH(NH2)COOH
Source
Purity
95%
Source
≥98.0% (NT)
Source
98%
Source
purum
Source
Grade