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Molecule
ID:77646
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₁₁NO₃
Molecular Mass
217.22064
Exact Mass
217.07389322
Charge
0
InChI
InChI=1S/C12H11NO3/c1-15-11-5-3-9(4-6-11)7-10(8-13)12(14)16-2/h3-7H,1-2H3
InChIKey
MCFCPVVFVXSZSK-UHFFFAOYSA-N
Canonic Smiles
COc1ccc(cc1)/C=C(\C(=O)OC)/C#N
Isomeric Smiles
O=C(OC)/C(=C\c1ccc(cc1)OC)/C#N
Calculated Properties
JChem
H Acceptors
3
H Donor
0
LogD (pH = 5.5)
2.169501
LogD (pH = 7.4)
2.169501
Log P
2.169501
Molar Refractivity
59.3458
Polarizability
22.497772
Polar Surface Area
59.32
Rotatable Bonds
4
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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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 name
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Synonyms
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IUPAC Traditional name
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MDL Number
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CAS Number
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PubChem CID
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PubChem SID
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Related Proteins
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From Data Sources
Bioactivity
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Data Source
Commercial Catalog
Apollo Scientific
OR15502
Academic Data
PubChem
678477
Names and Identifiers
IUPAC name
methyl 2-cyano-3-(4-methoxyphenyl)prop-2-enoate
Synonyms
Methyl (E)-2-cyano-3-(4-methoxyphenyl)acrylate
4-[(1E)-2-Cyano-3-methoxy-3-oxoprop-1-en-1-yl]anisole
Methyl trans-alpha-cyano-4-methoxycinnamate
Methyl (2E)-2-cyano-3-(4-methoxyphenyl)prop-2-enoate
IUPAC Traditional name
methyl 2-cyano-3-(4-methoxyphenyl)prop-2-enoate
Registration numbers
MDL Number
MFCD00630908
CAS Number
14479-58-4
PubChem CID
678477
PubChem SID
162042518
Properties
Safety Information
Storage Warning
Irritant
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay