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Molecule
ID:38963
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₄H₁₈FNO₄
Molecular Mass
283.2954232
Exact Mass
283.12198628
Charge
0
InChI
InChI=1S/C14H18FNO4/c1-14(2,3)20-13(19)16-11(12(17)18)8-9-5-4-6-10(15)7-9/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)/t11-/m1/s1
InChIKey
FPCCREICRYPTTL-LLVKDONJSA-N
Canonic Smiles
O=C(OC(C)(C)C)N[C@@H](C(=O)O)Cc1cccc(c1)F
Isomeric Smiles
c1c(cc(cc1)C[C@H](C(=O)O)NC(=O)OC(C)(C)C)F
Calculated Properties
JChem
Acid pKa
3.8336127
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
1.0426761
LogD (pH = 7.4)
-0.5342092
Log P
2.7124143
Molar Refractivity
70.2057
Polarizability
27.239302
Polar Surface Area
75.63
Rotatable Bonds
6
Lipinski's Rule of Five
true
Data Source
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Related Proteins
No Data Available
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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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IUPAC name
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CAS Number
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PubChem SID
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PubChem CID
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Product Information
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Molecular Spectra
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Sigma Aldrich
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Bioactivity
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Data Source
Commercial Catalog
Apollo Scientific
PC6045
Sigma Aldrich
14995
Bide Pharmatech
BD17628
Alfa Aesar
H51963
Matrix Scientific
041861
Academic Data
PubChem
7020836
Names and Identifiers
IUPAC Traditional name
(2R)-2-[(tert-butoxycarbonyl)amino]-3-(3-fluorophenyl)propanoic acid
IUPAC name
(2R)-2-{[(tert-butoxy)carbonyl]amino}-3-(3-fluorophenyl)propanoic acid
Synonyms
3-Fluoro-L-phenylalanine, N-BOC protected
(2S)-2-[(tert-Butoxycarbonyl)amino]-3-(3-fluorophenyl)propanoic acid
Boc-3-fluoro-D-phenylalanine
Boc-D-Phe(3-F)-OH
Boc-3-fluoro-D-phenylalanine
Boc-D-3-氟苯丙氨酸
(R)-N-Boc-3-Fluorophenylalanine
N-Boc-3-氟-D-苯基丙氨酸
Boc-D-Phe(3-F)-OH
N-Boc-3-fluoro-D-phenylalanine
Registration numbers
MDL Number
MFCD00672523
MFCD00672522
CAS Number
114873-11-9
114873-01-7
PubChem SID
24848990
161002270
PubChem CID
7020836
Properties
Safety Information
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Irritant/Keep Cold
Source
German water hazard class
3
Source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
Physical Property
Melting Point
79-85°C
Source
75-79°C
Source
Optical Rotation
[α]20/D -6.5±1°, c = 1% in methanol
Source
-6.5 (c=1 in methanol)
Source
Product Information
Empirical Formula (Hill Notation)
C14H18FNO4
Source
Purity
≥98.0% (TLC)
Source
98%
Source
Molecule Details
Sigma Aldrich
14995
Packaging
5 g in poly bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay