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Molecule
ID:116563
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₁H₁₀N₄OS₂
Molecular Mass
278.3533
Exact Mass
278.02960296
Charge
0
InChI
InChI=1S/C11H10N4OS2/c1-14-9(12-13-10(14)17)6-15-7-4-2-3-5-8(7)18-11(15)16/h2-5H,6H2,1H3,(H,13,17)
InChIKey
KVAYABJASYRGKL-UHFFFAOYSA-N
Canonic Smiles
Cn1c(=S)[nH]nc1Cn1c(=O)sc2c1cccc2
Isomeric Smiles
n1(c(=O)sc2c1cccc2)Cc1n(c(=S)[nH]n1)C
Calculated Properties
JChem
Acid pKa
7.8004055
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
2.1065905
LogD (pH = 7.4)
1.9759675
Log P
2.1085968
Molar Refractivity
75.3175
Polarizability
28.792805
Polar Surface Area
47.94
Rotatable Bonds
2
Lipinski's Rule of Five
true
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Molecular Spectra
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Molecule Details
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Bioactivity
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Data Source
Academic Data
PubChem
2049996
Commercial Catalog
Life Chemicals
F2147-0292
Names and Identifiers
IUPAC Traditional name
3-[(4-methyl-5-sulfanylidene-1H-1,2,4-triazol-3-yl)methyl]-1,3-benzothiazol-2-one
IUPAC name
3-[(4-methyl-5-sulfanylidene-4,5-dihydro-1H-1,2,4-triazol-3-yl)methyl]-2,3-dihydro-1,3-benzothiazol-2-one
Synonyms
3-[(4-methyl-5-thioxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)methyl]-1,3-benzothiazol-2(3H)-one
Registration numbers
MDL Number
MFCD05860971
PubChem CID
2049996
PubChem SID
162102231
Properties
Physical Property
Partition Coefficient
4.039
Source
Product Information
Purity
95+%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay