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Molecule
ID:22324
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₅ClN₂O₂
Molecular Mass
172.5691
Exact Mass
172.00395509
Charge
0
InChI
InChI=1S/C6H5ClN2O2/c1-4-2-6(7)8-3-5(4)9(10)11/h2-3H,1H3
InChIKey
HWZUMEVIIGNXGM-UHFFFAOYSA-N
Canonic Smiles
[O-][N+](=O)c1cnc(cc1C)Cl
Isomeric Smiles
[N+](=O)([O-])c1c(C)cc(nc1)Cl
Calculated Properties
JChem
H Acceptors
3
H Donor
0
LogD (pH = 5.5)
2.0332007
LogD (pH = 7.4)
2.0332007
Log P
2.0332007
Molar Refractivity
41.1289
Polarizability
15.124778
Polar Surface Area
56.03
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
•
RDKit
•
JChem
Data Source
Names and Identifiers
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IUPAC name
•
Synonyms
•
IUPAC Traditional name
Registration numbers
•
CAS Number
•
MDL Number
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PubChem SID
•
PubChem CID
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
Bioactivity
Names and Identifiers
IUPAC name
2-chloro-4-methyl-5-nitropyridine
Synonyms
2-Chloro-4-methyl-5-nitropyridine
2-Chloro-5-nitro-4-picoline
2-氯-5-硝基-4-甲基吡啶
2-Chloro-4-methyl-5-nitropyridine
IUPAC Traditional name
2-chloro-4-methyl-5-nitropyridine
Registration numbers
CAS Number
23056-33-9
MDL Number
MFCD00010688
PubChem SID
24857428
160985631
PubChem CID
345364
Molecule Details
Sigma Aldrich
290122
Packaging
1 g in glass bottle
Properties
Safety Information
Storage Warning
IRRITANT
Source
Irritant
Source
MSDS Link
Download link
Source
Download link
Source
TSCA Listed
false
Source
否
Source
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
dust mask type N95 (US), Eyeshields, Gloves
Source
3
Source
Warning
Source
P261
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-
P501
Source
36/37/38
Source
Irritant (Xi)
H315
-
H319
-
H335
Source
26
-
37/39
Source
26
-
37
-
60
Source
Product Information
98%
Source
97%
Source
95%
Source
C6H5ClN2O2
Source
Physical Property
91°C/5mm
Source
91 °C/5 mmHg(lit.)
Source
91°C
Source
>110°C
Source
113 °C
Source
235.4 °F
Source
113°C(235°F)
Source
Data Source
Commercial Catalog
Apollo Scientific
OR3149
Matrix Scientific
024705
Sigma Aldrich
290122
Enamine
EN300-97887
Bide Pharmatech
BD42482
Alfa Aesar
H60039
A&J Pharmtech
AJA-O12378
Academic Data
PubChem
345364
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Data Source
•
Commercial Catalog
•
Academic Data
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Source
Source
37-39°C
Source
37-39 °C(lit.)
Source
37 - 39°C
Source
37-39°C
Source
Hydrophobicity(logP)
1.729
Source
GHS Pictograms
Personal Protective Equipment
German water hazard class
GHS Signal Word
GHS Precautionary statements
Risk Statements
European Hazard Symbols
GHS Hazard statements
Safety Statements
Purity
Empirical Formula (Hill Notation)
Boiling Point
Flash Point
Melting Point