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Molecule
ID:11488
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₉N₃
Molecular Mass
159.18786
Exact Mass
159.0796473
Charge
0
InChI
InChI=1S/C9H9N3/c10-8-3-1-2-4-9(8)12-6-5-11-7-12/h1-7H,10H2
InChIKey
HVECTIQVQPUSEX-UHFFFAOYSA-N
Canonic Smiles
Nc1ccccc1n1cncc1
Isomeric Smiles
n1(c2c(N)cccc2)cncc1
Calculated Properties
JChem
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
0.3935258
LogD (pH = 7.4)
0.87521106
Log P
0.90748435
Molar Refractivity
58.7068
Polarizability
18.570034
Polar Surface Area
43.84
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
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Academic Data
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IUPAC name
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Synonyms
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IUPAC Traditional name
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MDL Number
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CAS Number
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PubChem CID
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PubChem SID
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Safety Information
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
References
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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
ChemBridge
4029918
Maybridge
CC32714
Matrix Scientific
008443
Life Chemicals
F2147-1111
Enamine
EN300-31568
Academic Data
PubChem
320166
Names and Identifiers
IUPAC name
2-(1H-imidazol-1-yl)aniline
Synonyms
2-Imidazol-1-yl-phenylamine
2-(1H-imidazol-1-yl)aniline
[2-(1H-imidazol-1-yl)phenyl]amine
IUPAC Traditional name
2-(imidazol-1-yl)aniline
Registration numbers
MDL Number
MFCD03274531
CAS Number
26286-54-4
PubChem CID
320166
PubChem SID
160974795
Properties
Safety Information
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
MSDS Link
Download link
Source
Product Information
Purity
97%
Source
95+%
Source
95%
Source
Physical Property
Partition Coefficient
1.012
Source
Hydrophobicity(logP)
0.87
Source
Melting Point
105 - 107°C
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay