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Molecule
ID:41520
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₁₀N₂O₃
Molecular Mass
230.2194
Exact Mass
230.06914219
Charge
0
InChI
InChI=1S/C12H10N2O3/c1-17-10-6-4-9(5-7-10)12-11(14(15)16)3-2-8-13-12/h2-8H,1H3
InChIKey
RFEKDBSKSCHAMP-UHFFFAOYSA-N
Canonic Smiles
COc1ccc(cc1)c1ncccc1[N+](=O)[O-]
Isomeric Smiles
c1cnc(c(c1)[N+](=O)[O-])c1ccc(cc1)OC
Calculated Properties
JChem
H Acceptors
4
H Donor
0
LogD (pH = 5.5)
2.570939
LogD (pH = 7.4)
2.5709617
Log P
2.570962
Molar Refractivity
62.4532
Polarizability
24.757978
Polar Surface Area
67.94
Rotatable Bonds
3
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
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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
•
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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CAS Number
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PubChem CID
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PubChem SID
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
044664
Apollo Scientific
OR14218
Key Organics
4Y-0710
Academic Data
PubChem
2763995
Names and Identifiers
IUPAC Traditional name
2-(4-methoxyphenyl)-3-nitropyridine
Synonyms
2-(4-Methoxyphenyl)-3-nitropyridine
IUPAC name
2-(4-methoxyphenyl)-3-nitropyridine
Registration numbers
MDL Number
MFCD06200969
CAS Number
182925-45-7
PubChem CID
2763995
PubChem SID
162046283
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
MSDS Link
Download link
Source
TSCA Listed
false
Source
Storage Warning
IRRITANT
Source
Irritant
Source
Physical Property
Melting Point
88-92°C
Source
88 - 92 °C
Source
Product Information
>95%
Source
> 95%
Source
Purity