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Molecule
ID:27919
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₁₀N₄S
Molecular Mass
206.2675
Exact Mass
206.06261734
Charge
0
InChI
InChI=1S/C9H10N4S/c1-2-13-8(11-12-9(13)14)7-3-5-10-6-4-7/h3-6H,2H2,1H3,(H,12,14)
InChIKey
ABRXECVGFQUVGO-UHFFFAOYSA-N
Canonic Smiles
CCn1c(S)nnc1c1ccncc1
Isomeric Smiles
n1(c(nnc1S)c1ccncc1)CC
Calculated Properties
JChem
Acid pKa
7.747208
H Acceptors
3
H Donor
1
LogD (pH = 5.5)
1.0479983
LogD (pH = 7.4)
0.9052505
Log P
1.0593631
Molar Refractivity
69.3021
Polarizability
22.303112
Polar Surface Area
43.6
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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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
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RDKit
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Product Information
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Molecular Spectra
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References
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
030484
Enamine
EN300-03203
Academic Data
PubChem
758273
Names and Identifiers
IUPAC name
4-ethyl-5-(pyridin-4-yl)-4H-1,2,4-triazole-3-thiol
IUPAC Traditional name
4-ethyl-5-(pyridin-4-yl)-1,2,4-triazole-3-thiol
Synonyms
4-Ethyl-5-pyridin-4-yl-4H-1,2,4-triazole-3-thiol
4-Ethyl-5-pyridin-4-yl-4H-[1,2,4]triazole-3-thiol
Registration numbers
PubChem CID
758273
PubChem SID
160991226
MDL Number
MFCD03286275
CAS Number
26029-01-6
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
MSDS Link
Download link
Source
Physical Property
Melting Point
140 - 142°C
Source
Hydrophobicity(logP)
0.978
Source
Product Information
95%
Source
Purity