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Molecule
ID:9685
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₈FNO₃
Molecular Mass
209.1738232
Exact Mass
209.04882134
Charge
0
InChI
InChI=1S/C10H8FNO3/c11-7-1-3-8(4-2-7)12-9(13)5-6-10(14)15/h1-6H,(H,12,13)(H,14,15)/b6-5+
InChIKey
NRDZVHHPNZDWRA-AATRIKPKSA-N
Canonic Smiles
O=C(Nc1ccc(cc1)F)/C=C/C(=O)O
Isomeric Smiles
c1c(ccc(c1)NC(=O)/C=C/C(=O)O)F
Calculated Properties
JChem
Acid pKa
2.961061
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
-0.9618517
LogD (pH = 7.4)
-1.9429471
Log P
1.5360895
Molar Refractivity
53.1007
Polarizability
18.944633
Polar Surface Area
66.4
Rotatable Bonds
3
Lipinski's Rule of Five
true
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Molecule Details
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Data Source
Commercial Catalog
Apollo Scientific
PC32261
Matrix Scientific
006102
Enamine
EN300-62655
Academic Data
PubChem
686484
Names and Identifiers
IUPAC name
(2E)-3-[(4-fluorophenyl)carbamoyl]prop-2-enoic acid
3-[(4-fluorophenyl)carbamoyl]prop-2-enoic acid
Synonyms
N-(4-Fluorophenyl)maleamic acid
4-(4-fluoroanilino)-4-oxobut-2-enoic acid
3-[(4-fluorophenyl)carbamoyl]prop-2-enoic acid
IUPAC Traditional name
(2E)-3-[(4-fluorophenyl)carbamoyl]prop-2-enoic acid
3-[(4-fluorophenyl)carbamoyl]prop-2-enoic acid
Registration numbers
MDL Number
MFCD00029808
MFCD00082643
CAS Number
60252-79-1
PubChem SID
160972992
PubChem CID
686484
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Physical Property
Melting Point
209°C
Source
Hydrophobicity(logP)
1.386
Source
Product Information
Purity
97%
Source
95%
Source
Safety Information
MSDS Link
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Source
false
Source
IRRITANT
Source
TSCA Listed
Storage Warning