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Molecule
ID:51482
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₆N₄S
Molecular Mass
178.21434
Exact Mass
178.03131721
Charge
0
InChI
InChI=1S/C7H6N4S/c8-7-10-6(11-12-7)5-2-1-3-9-4-5/h1-4H,(H2,8,10,11)
InChIKey
DZQRFUXSKCTOTP-UHFFFAOYSA-N
Canonic Smiles
Nc1snc(n1)c1cccnc1
Isomeric Smiles
n1c(nsc1N)c1cnccc1
Calculated Properties
JChem
Acid pKa
14.263796
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
1.2020818
LogD (pH = 7.4)
1.2090943
Log P
1.2091846
Molar Refractivity
58.5076
Polarizability
17.77028
Polar Surface Area
64.69
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
No Data Available
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Molecular Spectra
No Data Available
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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
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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IUPAC Traditional name
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Synonyms
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IUPAC 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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Safety Information
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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
•
PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
055453
Key Organics
DE-0705
Enamine
EN300-118281
Academic Data
PubChem
21486262
Names and Identifiers
IUPAC Traditional name
3-(pyridin-3-yl)-1,2,4-thiadiazol-5-amine
Synonyms
3-(3-Pyridinyl)-1,2,4-thiadiazol-5-amine
3-(pyridin-3-yl)-1,2,4-thiadiazol-5-amine
IUPAC name
3-(pyridin-3-yl)-1,2,4-thiadiazol-5-amine
Registration numbers
MDL Number
MFCD12137242
PubChem SID
162056245
PubChem CID
21486262
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
TSCA Listed
false
Source
MSDS Link
Download link
Source
Storage Warning
IRRITANT
Source
Physical Property
Melting Point
244-246°C
Source
244 - 246 °C
Source
0.281
Source
Product Information
>95%
Source
95%
Source
Hydrophobicity(logP)
Purity