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Molecule
ID:122918
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₅H₁₂O₂
Molecular Mass
224.25458
Exact Mass
224.08372962
Charge
0
InChI
InChI=1S/C15H12O2/c16-15(17)14(13-9-5-2-6-10-13)11-12-7-3-1-4-8-12/h1-11H,(H,16,17)/b14-11-
InChIKey
BIDDLDNGQCUOJQ-KAMYIIQDSA-N
Canonic Smiles
OC(=O)/C(=C\c1ccccc1)/c1ccccc1
Isomeric Smiles
C(=C\c1ccccc1)(\C(=O)O)/c1ccccc1
Calculated Properties
JChem
Acid pKa
3.7405453
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
2.044541
LogD (pH = 7.4)
0.5154929
Log P
3.804174
Molar Refractivity
67.512
Polarizability
25.871016
Polar Surface Area
37.3
Rotatable Bonds
3
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Properties
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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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RDKit
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IUPAC name
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IUPAC Traditional name
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Synonyms
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
References
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
InterBioScreen
BB_SC-5587
Sigma Aldrich
P22001
Enamine
EN300-17442
Academic Data
PubChem
700622
Names and Identifiers
IUPAC name
(2Z)-2,3-diphenylprop-2-enoic acid
2,3-diphenylprop-2-enoic acid
IUPAC Traditional name
(2Z)-2,3-diphenylprop-2-enoic acid
2,3-diphenylprop-2-enoic acid
Synonyms
(Z)-2,3-diphenylacrylic acid
α-苯基肉桂酸
α-Phenylcinnamic acid
alpha-Phenylcinnamic acid
2,3-diphenylprop-2-enoic acid
Registration numbers
EC Number
202-069-4
PubChem SID
24898288
162217271
MDL Number
MFCD00004252
CAS Number
91-48-5
PubChem CID
700622
Molecule Details
Sigma Aldrich
P22001
Packaging
25 g in poly bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Product Information
Linear Formula
C6H5CH=C(C6H5)CO2H
Source
Purity
97%
Source
95%
Source
Safety Information
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Source
German water hazard class
3
Source
Download link
Source
Physical Property
172-174 °C(lit.)
Source
172 - 174°C
Source
3.587
Source
Related Proteins
Registration numbers
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MDL Number
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Melting Point
Hydrophobicity(logP)
No Data Available
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