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Molecule
ID:57944
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₄H₁₄N₂O₂
Molecular Mass
242.27316
Exact Mass
242.1055277
Charge
0
InChI
InChI=1S/C14H14N2O2/c1-18-11-8-6-10(7-9-11)16-14(17)12-4-2-3-5-13(12)15/h2-9H,15H2,1H3,(H,16,17)
InChIKey
VOUMPTOODFUGMO-UHFFFAOYSA-N
Canonic Smiles
COc1ccc(cc1)NC(=O)c1ccccc1N
Isomeric Smiles
C(=O)(c1c(N)cccc1)Nc1ccc(cc1)OC
Calculated Properties
JChem
Acid pKa
12.136202
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
2.7282982
LogD (pH = 7.4)
2.7285228
Log P
2.7285335
Molar Refractivity
72.7551
Polarizability
26.592268
Polar Surface Area
64.35
Rotatable Bonds
3
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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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
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IUPAC Traditional name
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Synonyms
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IUPAC name
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PubChem CID
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Product Information
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Physical Property
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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
063121
Enamine
EN300-05555
Academic Data
PubChem
478820
Names and Identifiers
IUPAC Traditional name
2-amino-N-(4-methoxyphenyl)benzamide
Synonyms
2-Amino-N-(4-methoxyphenyl)benzamide
2-Amino-N-(4-methoxy-phenyl)-benzamide
IUPAC name
2-amino-N-(4-methoxyphenyl)benzamide
Registration numbers
CAS Number
20878-54-0
MDL Number
MFCD00434408
PubChem CID
478820
PubChem SID
162062707
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
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
2.418
Source
Hydrophobicity(logP)