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Molecule
ID:120897
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₈N₄
Molecular Mass
160.17592
Exact Mass
160.07489628
Charge
0
InChI
InChI=1S/C8H8N4/c9-7-3-1-6(2-4-7)8-10-5-11-12-8/h1-5H,9H2,(H,10,11,12)
InChIKey
KTEQHOVTBRZQPC-UHFFFAOYSA-N
Canonic Smiles
Nc1ccc(cc1)c1n[nH]cn1
Isomeric Smiles
n1c(n[nH]c1)c1ccc(N)cc1
Calculated Properties
JChem
Acid pKa
10.113157
H Acceptors
3
H Donor
2
LogD (pH = 5.5)
0.08544652
LogD (pH = 7.4)
0.08934326
Log P
0.09016843
Molar Refractivity
59.031
Polarizability
17.665424
Polar Surface Area
67.59
Rotatable Bonds
1
Lipinski's Rule of Five
true
Data Source
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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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IUPAC Traditional name
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Synonyms
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IUPAC name
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PubChem CID
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PubChem SID
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MDL Number
Properties
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Physical Property
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
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PubChem Literature
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
InterBioScreen
BB_SC-10261
Enamine
EN300-74655
Academic Data
PubChem
3052732
Names and Identifiers
IUPAC Traditional name
4-(1H-1,2,4-triazol-3-yl)aniline
4-(4H-1,2,4-triazol-3-yl)aniline
Synonyms
4-(1H-1,2,4-triazol-3-yl)aniline
4-(4H-1,2,4-triazol-3-yl)aniline
IUPAC name
4-(1H-1,2,4-triazol-3-yl)aniline
4-(4H-1,2,4-triazol-3-yl)aniline
Registration numbers
PubChem CID
3052732
PubChem SID
162215250
MDL Number
MFCD07643239
Properties
Physical Property
Hydrophobicity(logP)
0.245
Source
Melting Point
203 - 205°C
Source
Product Information
Purity
95%
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay