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Molecule
ID:41543
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₃H₁₀N₂O₄
Molecular Mass
258.2295
Exact Mass
258.06405681
Charge
0
InChI
InChI=1S/C13H10N2O4/c1-19-13(16)10-6-4-9(5-7-10)12-11(15(17)18)3-2-8-14-12/h2-8H,1H3
InChIKey
MXJLOXZMDUQVLN-UHFFFAOYSA-N
Canonic Smiles
COC(=O)c1ccc(cc1)c1ncccc1[N+](=O)[O-]
Isomeric Smiles
c1cnc(c(c1)[N+](=O)[O-])c1ccc(cc1)C(=O)OC
Calculated Properties
JChem
H Acceptors
4
H Donor
0
LogD (pH = 5.5)
2.7320983
LogD (pH = 7.4)
2.73211
Log P
2.7321103
Molar Refractivity
68.0153
Polarizability
26.673681
Polar Surface Area
85.01
Rotatable Bonds
4
Lipinski's Rule of Five
true
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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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From Data Sources
Bioactivity
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PubChem BioAssay
Data Source
Commercial Catalog
Matrix Scientific
044691
Apollo Scientific
OR15109
Key Organics
4Z-0708
Academic Data
PubChem
18526003
Names and Identifiers
IUPAC Traditional name
methyl 4-(3-nitropyridin-2-yl)benzoate
Synonyms
Methyl 4-(3-nitropyridin-2-yl)benzoate
Methyl 4-(3-nitro-2-pyridinyl)benzenecarboxylate
IUPAC name
methyl 4-(3-nitropyridin-2-yl)benzoate
Registration numbers
MDL Number
MFCD08443945
PubChem CID
18526003
PubChem SID
162046306
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Safety Information
Storage Warning
IRRITANT
Source
Irritant
Source
TSCA Listed
false
Source
MSDS Link
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Source
Product Information
Purity
>95%
Source
Physical Property
82-84°C
Source
82 - 84 °C
Source
Melting Point