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Molecule
ID:116217
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₀H₁₁N₃O
Molecular Mass
189.21384
Exact Mass
189.09021199
Charge
0
InChI
InChI=1S/C10H11N3O/c1-6-3-4-8(7(2)5-6)9-12-13-10(11)14-9/h3-5H,1-2H3,(H2,11,13)
InChIKey
WMTJZHAGZHSWNQ-UHFFFAOYSA-N
Canonic Smiles
Cc1ccc(c(c1)C)c1nnc(o1)N
Isomeric Smiles
c1(oc(nn1)N)c1c(cc(cc1)C)C
Calculated Properties
JChem
Acid pKa
12.979237
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
1.8616217
LogD (pH = 7.4)
1.8616215
Log P
1.8616226
Molar Refractivity
66.3413
Polarizability
20.375034
Polar Surface Area
64.94
Rotatable Bonds
1
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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IUPAC Traditional name
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IUPAC name
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Synonyms
Registration numbers
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MDL Number
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CAS Number
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PubChem SID
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PubChem CID
Properties
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Physical Property
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Product Information
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
ChemBridge
4025433
Life Chemicals
F2146-0046
Enamine
EN300-53799
Academic Data
PubChem
20120079
Names and Identifiers
IUPAC Traditional name
5-(2,4-dimethylphenyl)-1,3,4-oxadiazol-2-amine
IUPAC name
5-(2,4-dimethylphenyl)-1,3,4-oxadiazol-2-amine
Synonyms
5-(2,4-dimethylphenyl)-1,3,4-oxadiazol-2-amine
Registration numbers
MDL Number
MFCD09815535
CAS Number
902137-22-8
PubChem SID
162100884
PubChem CID
20120079
Properties
Physical Property
Partition Coefficient
2.85
Source
Hydrophobicity(logP)
1.513
Source
Product Information
Purity
95+%
Source
95%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay