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Molecule
ID:51348
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₁₁NO₂
Molecular Mass
177.19984
Exact Mass
177.0789786
Charge
0
InChI
InChI=1S/C10H11NO2/c1-2-13-10(12)4-3-9-5-7-11-8-6-9/h3-8H,2H2,1H3/b4-3+
InChIKey
ABZPCWYIRGIXJP-ONEGZZNKSA-N
Canonic Smiles
CCOC(=O)/C=C/c1ccncc1
Isomeric Smiles
C(=C\c1ccncc1)/C(=O)OCC
Calculated Properties
JChem
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
1.5360177
LogD (pH = 7.4)
1.6526753
Log P
1.6544492
Molar Refractivity
50.4207
Polarizability
19.229458
Polar Surface Area
39.19
Rotatable Bonds
4
Lipinski's Rule of Five
true
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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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MDL Number
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Molecular Spectra
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
054888
Key Organics
AE-0249
Academic Data
PubChem
10352231
Names and Identifiers
IUPAC name
ethyl (2E)-3-(pyridin-4-yl)prop-2-enoate
Synonyms
Ethyl (E)-3-(4-pyridinyl)-2-propenoate
IUPAC Traditional name
ethyl (2E)-3-(pyridin-4-yl)prop-2-enoate
Registration numbers
CAS Number
24489-96-1
MDL Number
MFCD07778427
PubChem CID
10352231
PubChem SID
162056111
Properties
Safety Information
MSDS Link
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Source
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
Product Information
Purity
>95%
Source
Physical Property
Melting Point
62-64°C
Source
62 - 64 °C
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay