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Molecule
ID:118147
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₉N₃O₃S
Molecular Mass
239.25106
Exact Mass
239.03646216
Charge
0
InChI
InChI=1S/C9H9N3O3S/c1-16(13,14)7-4-2-3-6(5-7)8-11-12-9(10)15-8/h2-5H,1H3,(H2,10,12)
InChIKey
UUYSHEKWLUMFIY-UHFFFAOYSA-N
Canonic Smiles
Nc1nnc(o1)c1cccc(c1)S(=O)(=O)C
Isomeric Smiles
o1c(nnc1N)c1cc(S(=O)(=O)C)ccc1
Calculated Properties
JChem
Acid pKa
12.865865
H Acceptors
5
H Donor
1
LogD (pH = 5.5)
-0.32491177
LogD (pH = 7.4)
-0.32491302
Log P
-0.32491162
Molar Refractivity
70.2625
Polarizability
22.902378
Polar Surface Area
99.08
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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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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Academic Data
Names and Identifiers
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IUPAC name
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IUPAC Traditional name
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Synonyms
Registration numbers
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CAS Number
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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
F2182-0015
Academic Data
PubChem
18070127
Names and Identifiers
IUPAC name
5-(3-methanesulfonylphenyl)-1,3,4-oxadiazol-2-amine
IUPAC Traditional name
5-(3-methanesulfonylphenyl)-1,3,4-oxadiazol-2-amine
Synonyms
5-[3-(methylsulfonyl)phenyl]-1,3,4-oxadiazol-2-amine
Registration numbers
CAS Number
1016764-70-7
MDL Number
MFCD09804361
PubChem SID
162098102
PubChem CID
18070127
Properties
Product Information
Purity
95+%
Source
Physical Property
Partition Coefficient
1.459
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay