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Molecule
ID:25030
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₇N₅
Molecular Mass
161.16398
Exact Mass
161.07014525
Charge
0
InChI
InChI=1S/C7H7N5/c8-6-1-3-7(4-2-6)12-5-9-10-11-12/h1-5H,8H2
InChIKey
JRRAUWWVBVECPY-UHFFFAOYSA-N
Canonic Smiles
Nc1ccc(cc1)n1cnnn1
Isomeric Smiles
n1(nnnc1)c1ccc(N)cc1
Calculated Properties
JChem
H Acceptors
4
H Donor
1
LogD (pH = 5.5)
0.15298457
LogD (pH = 7.4)
0.1813699
Log P
0.1817442
Molar Refractivity
47.6933
Polarizability
16.794886
Polar Surface Area
69.62
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
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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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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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CAS Number
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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
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
027559
ChemBridge
4002011
Life Chemicals
F2121-0004
Enamine
EN300-34129
Academic Data
PubChem
571640
Names and Identifiers
IUPAC Traditional name
4-(1,2,3,4-tetrazol-1-yl)aniline
Synonyms
4-(1H-Tetrazol-1-yl)aniline
[4-(1H-tetrazol-1-yl)phenyl]amine
4-(1H-1,2,3,4-tetrazol-1-yl)aniline
IUPAC name
4-(1H-1,2,3,4-tetrazol-1-yl)aniline
Registration numbers
CAS Number
14213-13-9
MDL Number
MFCD02746184
PubChem SID
160988337
PubChem CID
571640
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
MSDS Link
Download link
Source
Storage Warning
IRRITANT
Source
TSCA Listed
false
Source
Physical Property
Partition Coefficient
-0.359
Source
Hydrophobicity(logP)
0.672
Source
140 - 142°C
Source
Product Information
95+%
Source
95%
Source
Melting Point
Purity