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Molecule
ID:11364
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₁₄N₂O₂
Molecular Mass
230.26246
Exact Mass
230.1055277
Charge
0
InChI
InChI=1S/C13H14N2O2/c1-9-12(13(16)17)10(2)15(14-9)8-11-6-4-3-5-7-11/h3-7H,8H2,1-2H3,(H,16,17)
InChIKey
QBQWUFSHKRRJPB-UHFFFAOYSA-N
Canonic Smiles
OC(=O)c1c(C)nn(c1C)Cc1ccccc1
Isomeric Smiles
c1(c(n(nc1C)Cc1ccccc1)C)C(=O)O
Calculated Properties
JChem
Acid pKa
1.9726939
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-0.3241821
LogD (pH = 7.4)
-1.3570377
Log P
1.5903585
Molar Refractivity
76.5714
Polarizability
24.352661
Polar Surface Area
55.12
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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References
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Bioactivity
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General Information
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IUPAC Traditional name
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Product Information
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Molecular Spectra
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References
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
008313
Life Chemicals
F3379-1062
InterBioScreen
BB_SC-7658
ChemBridge
5100343
Enamine
EN300-05897
Academic Data
PubChem
2826762
Names and Identifiers
IUPAC name
1-benzyl-3,5-dimethyl-1H-pyrazole-4-carboxylic acid
IUPAC Traditional name
1-benzyl-3,5-dimethylpyrazole-4-carboxylic acid
Synonyms
1-Benzyl-3,5-dimethyl-1H-pyrazole-4-carboxylic acid
Registration numbers
CAS Number
108444-25-3
MDL Number
MFCD00447225
PubChem SID
160974671
PubChem CID
2826762
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
MSDS Link
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Source
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
Physical Property
Partition Coefficient
1.862
Source
Hydrophobicity(logP)
2.108
Source
137 - 139°C
Source
Product Information
95+%
Source
95%
Source
Melting Point
Purity