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Molecule
ID:36749
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₇H₁₄N₂O₂S
Molecular Mass
310.37026
Exact Mass
310.0775987
Charge
0
InChI
InChI=1S/C17H14N2O2S/c1-21-15-10-6-5-7-12(15)11-14-16(20)19(17(22)18-14)13-8-3-2-4-9-13/h2-11H,1H3,(H,18,22)/b14-11+
InChIKey
JSEQNNYGDRRNFM-SDNWHVSQSA-N
Canonic Smiles
COc1ccccc1/C=C\1/N=C(N(C1=O)c1ccccc1)S
Isomeric Smiles
N1(C(=N/C(=C/c2c(OC)cccc2)/C1=O)S)c1ccccc1
Calculated Properties
JChem
Acid pKa
6.135342
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
3.6513057
LogD (pH = 7.4)
2.8130498
Log P
3.7345846
Molar Refractivity
89.5137
Polarizability
33.917244
Polar Surface Area
41.9
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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Bioactivity
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General Information
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IUPAC name
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Bioactivity
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Data Source
Academic Data
PubChem
5925399
Commercial Catalog
Matrix Scientific
039542
Names and Identifiers
Synonyms
(5E)-2-Mercapto-5-(2-methoxybenzylidene)-3-phenyl-3,5-dihydro-4H-imidazol-4-one
IUPAC name
(4E)-4-[(2-methoxyphenyl)methylidene]-1-phenyl-2-sulfanyl-4,5-dihydro-1H-imidazol-5-one
IUPAC Traditional name
(5E)-5-[(2-methoxyphenyl)methylidene]-3-phenyl-2-sulfanylimidazol-4-one
Registration numbers
MDL Number
MFCD12028005
PubChem CID
5925399
PubChem SID
161000056
Properties
Safety Information
MSDS Link
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Source
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay