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Molecule
ID:27583
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₁₁NO₄
Molecular Mass
233.22004
Exact Mass
233.06880784
Charge
0
InChI
InChI=1S/C12H11NO4/c1-8(14)9-2-4-10(5-3-9)13-11(15)6-7-12(16)17/h2-7H,1H3,(H,13,15)(H,16,17)/b7-6+
InChIKey
CWSPWHGWDJSNIB-VOTSOKGWSA-N
Canonic Smiles
OC(=O)/C=C/C(=O)Nc1ccc(cc1)C(=O)C
Isomeric Smiles
C(=O)(/C=C/C(=O)O)Nc1ccc(C(=O)C)cc1
Calculated Properties
JChem
Acid pKa
3.2427135
H Acceptors
4
H Donor
2
LogD (pH = 5.5)
-1.2860444
LogD (pH = 7.4)
-2.486585
Log P
0.9510351
Molar Refractivity
63.2871
Polarizability
22.944818
Polar Surface Area
83.47
Rotatable Bonds
4
Lipinski's Rule of Five
true
Data Source
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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
Calculated Properties
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RDKit
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JChem
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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IUPAC name
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Synonyms
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IUPAC Traditional name
Registration numbers
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CAS Number
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MDL Number
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PubChem CID
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PubChem SID
Properties
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Safety Information
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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
Matrix Scientific
030143
Key Organics
6T-0030
Academic Data
PubChem
708611
Names and Identifiers
IUPAC name
(2E)-3-[(4-acetylphenyl)carbamoyl]prop-2-enoic acid
Synonyms
4-(4-Acetylanilino)-4-oxo-2-butenoic acid
IUPAC Traditional name
(2E)-3-[(4-acetylphenyl)carbamoyl]prop-2-enoic acid
Registration numbers
CAS Number
24870-12-0
MDL Number
MFCD00174964
PubChem CID
708611
PubChem SID
160990890
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
TSCA Listed
false
Source
MSDS Link
Download link
Source
Storage Warning
IRRITANT
Source
Product Information
Purity
>95%
Source
Physical Property
206 - 209 °C
Source
Melting Point