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Molecule
ID:115860
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/c1-8-3-2-4-9(5-8)11-14-12(16-15-11)10-6-13-7-10/h2-5,10,13H,6-7H2,1H3
InChIKey
KCFPETCSEALGPN-UHFFFAOYSA-N
Canonic Smiles
Cc1cccc(c1)c1noc(n1)C1CNC1
Isomeric Smiles
n1c(noc1C1CNC1)c1cc(ccc1)C
Calculated Properties
JChem
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
-0.85133684
LogD (pH = 7.4)
0.6058497
Log P
2.3244166
Molar Refractivity
72.4887
Polarizability
23.718391
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
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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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Academic Data
Names and Identifiers
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Synonyms
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IUPAC name
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IUPAC Traditional name
Registration numbers
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MDL Number
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PubChem SID
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PubChem CID
Properties
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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
Life Chemicals
F2145-0234
Academic Data
PubChem
49657873
Names and Identifiers
Synonyms
5-azetidin-3-yl-3-(3-methylphenyl)-1,2,4-oxadiazole hydrochloride
IUPAC name
5-(azetidin-3-yl)-3-(3-methylphenyl)-1,2,4-oxadiazole
IUPAC Traditional name
5-(azetidin-3-yl)-3-(3-methylphenyl)-1,2,4-oxadiazole
Registration numbers
MDL Number
MFCD16652988
PubChem SID
162100761
PubChem CID
49657873
Properties
Product Information
Salt Data
HCl
Source
Purity
95+%
Source
Physical Property
Partition Coefficient
1.481
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay