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Molecule
ID:69749
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₉NO₃
Molecular Mass
167.16196
Exact Mass
167.05824315
Charge
0
InChI
InChI=1S/C8H9NO3/c1-6-3-4-7(9(10)11)5-8(6)12-2/h3-5H,1-2H3
InChIKey
WVQGZNRUEVFXKR-UHFFFAOYSA-N
Canonic Smiles
COc1cc(ccc1C)[N+](=O)[O-]
Isomeric Smiles
COc1c(ccc(c1)[N+](=O)[O-])C
Calculated Properties
JChem
H Acceptors
3
H Donor
0
LogD (pH = 5.5)
2.26898
LogD (pH = 7.4)
2.26898
Log P
2.26898
Molar Refractivity
43.8829
Polarizability
16.504642
Polar Surface Area
52.37
Rotatable Bonds
2
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
•
RDKit
•
JChem
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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IUPAC name
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Synonyms
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IUPAC Traditional name
Registration numbers
Properties
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Safety Information
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
References
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PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR6224
Sigma Aldrich
213187
Matrix Scientific
075253
Bide Pharmatech
BD11206
Academic Data
PubChem
83159
Names and Identifiers
IUPAC name
2-methoxy-1-methyl-4-nitrobenzene
Synonyms
2-Methyl-5-nitroanisole
2-Methoxy-4-nitrotoluene
2-Methyl-5-nitroanisole
5-硝基-2-甲基苯甲醚
IUPAC Traditional name
2-methoxy-1-methyl-4-nitrobenzene
Registration numbers
PubChem CID
83159
MDL Number
MFCD00043912
PubChem SID
162035474
24852771
CAS Number
13120-77-9
EC Number
236-048-6
Properties
Safety Information
Storage Warning
IRRITANT
Source
Irritant
Source
MSDS Link
Download link
Source
Download link
Source
TSCA Listed
false
Source
GHS Precautionary statements
P305+P351+P338
Source
European Hazard Symbols
Harmful (Xn)
Source
German water hazard class
3
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Hazard statements
H302
-
H319
Source
Risk Statements
22
Source
GHS Signal Word
Warning
Source
Product Information
Purity
95+%
Source
99%
Source
Linear Formula
CH3C6H3(NO2)OCH3
Source
Physical Property
Melting Point
69-71°C
Source
69-71 °C(lit.)
Source
Molecule Details
Sigma Aldrich
213187
Packaging
1, 10 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Registration numbers
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PubChem CID
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MDL Number
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PubChem SID
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CAS Number
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EC Number