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Molecule
ID:115859
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₁₃N₃O
Molecular Mass
215.25112
Exact Mass
215.10586205
Charge
0
InChI
InChI=1S/C12H13N3O/c1-8-4-2-3-5-10(8)11-14-12(16-15-11)9-6-13-7-9/h2-5,9,13H,6-7H2,1H3
InChIKey
UOXPBNSMDDIYOR-UHFFFAOYSA-N
Canonic Smiles
Cc1ccccc1c1noc(n1)C1CNC1
Isomeric Smiles
n1c(noc1C1CNC1)c1c(C)cccc1
Calculated Properties
JChem
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-0.85132194
LogD (pH = 7.4)
0.6058894
Log P
2.3244166
Molar Refractivity
72.4887
Polarizability
23.718456
Polar Surface Area
50.95
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
No Data Available
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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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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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MDL Number
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PubChem CID
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PubChem SID
Properties
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Academic Data
PubChem
49657872
Commercial Catalog
Life Chemicals
F2145-0233
Names and Identifiers
IUPAC name
5-(azetidin-3-yl)-3-(2-methylphenyl)-1,2,4-oxadiazole
Synonyms
5-azetidin-3-yl-3-(2-methylphenyl)-1,2,4-oxadiazole hydrochloride
IUPAC Traditional name
5-(azetidin-3-yl)-3-(2-methylphenyl)-1,2,4-oxadiazole
Registration numbers
MDL Number
MFCD16652987
PubChem CID
49657872
PubChem SID
162100922
Properties
Product Information
Purity
95+%
Source
Salt Data
HCl
Source
Physical Property
Partition Coefficient
1.442
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay