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Molecule
ID:40533
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₁₁FN₂O₂
Molecular Mass
234.2263432
Exact Mass
234.08045582
Charge
0
InChI
InChI=1S/C12H11FN2O2/c1-7-11(12(16)17)8(2)15(14-7)10-5-3-9(13)4-6-10/h3-6H,1-2H3,(H,16,17)
InChIKey
NKCDCNWWMFTZPW-UHFFFAOYSA-N
Canonic Smiles
Fc1ccc(cc1)n1nc(c(c1C)C(=O)O)C
Isomeric Smiles
n1(nc(c(c1C)C(=O)O)C)c1ccc(cc1)F
Calculated Properties
JChem
Acid pKa
3.220484
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-0.25316834
LogD (pH = 7.4)
-1.2816691
Log P
1.7705983
Molar Refractivity
61.6335
Polarizability
22.960508
Polar Surface Area
55.12
Rotatable Bonds
2
Lipinski's Rule of Five
true
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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Data Source
Commercial Catalog
Key Organics
1R-0666
Life Chemicals
F2130-0198
Matrix Scientific
043557
Enamine
EN300-13205
Academic Data
PubChem
1491355
Names and Identifiers
IUPAC Traditional name
1-(4-fluorophenyl)-3,5-dimethylpyrazole-4-carboxylic acid
Synonyms
1-(4-Fluorophenyl)-3,5-dimethyl-1H-pyrazole-4-carboxylic acid
IUPAC name
1-(4-fluorophenyl)-3,5-dimethyl-1H-pyrazole-4-carboxylic acid
Registration numbers
MDL Number
MFCD02083021
CAS Number
288251-63-8
PubChem SID
162045296
PubChem CID
1491355
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
MSDS Link
Download link
Source
Physical Property
Melting Point
215-217°C
Source
215 - 217 °C
Source
15 - 17°C
Source
1.881
Source
2.447
Source
Product Information
>95%
Source
95+%
Source
95%
Source
Partition Coefficient
Hydrophobicity(logP)
Purity