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Molecule
ID:14162
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₁₁N₃O
Molecular Mass
213.23524
Exact Mass
213.09021199
Charge
0
InChI
InChI=1S/C12H11N3O/c13-10-3-1-2-4-11(10)15-12(16)9-5-7-14-8-6-9/h1-8H,13H2,(H,15,16)
InChIKey
QBPHVELTLHFPNF-UHFFFAOYSA-N
Canonic Smiles
O=C(c1ccncc1)Nc1ccccc1N
Isomeric Smiles
c1(NC(=O)c2ccncc2)c(cccc1)N
Calculated Properties
JChem
Acid pKa
11.7750025
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
1.0163003
LogD (pH = 7.4)
1.0184866
Log P
1.0185323
Molar Refractivity
64.135
Polarizability
23.178343
Polar Surface Area
68.01
Rotatable Bonds
2
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
Calculated Properties
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RDKit
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IUPAC Traditional name
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Synonyms
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IUPAC name
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MDL Number
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PubChem CID
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Physical Property
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Product Information
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Molecular Spectra
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References
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
011678
Enamine
EN300-43578
Academic Data
PubChem
1133081
Names and Identifiers
IUPAC Traditional name
N-(2-aminophenyl)pyridine-4-carboxamide
Synonyms
N-(2-Amino-phenyl)-isonicotinamide
N-(2-aminophenyl)pyridine-4-carboxamide
IUPAC name
N-(2-aminophenyl)pyridine-4-carboxamide
Registration numbers
CAS Number
105101-25-5
MDL Number
MFCD02585709
PubChem CID
1133081
PubChem SID
160977469
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
MSDS Link
Download link
Source
Physical Property
Melting Point
179 - 181°C
Source
Hydrophobicity(logP)
0.67
Source
Product Information
95%
Source
Purity