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Molecule
ID:88795
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₉H₆ClN
Molecular Mass
163.60364
Exact Mass
163.01887688
Charge
0
InChI
InChI=1S/C9H6ClN/c10-8-4-1-5-9-7(8)3-2-6-11-9/h1-6H
InChIKey
HJSRGOVAIOPERP-UHFFFAOYSA-N
Canonic Smiles
Clc1cccc2c1cccn2
Isomeric Smiles
n1cccc2c(cccc12)Cl
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
2.7279394
LogD (pH = 7.4)
2.7348561
Log P
2.734945
Molar Refractivity
44.7841
Polarizability
18.839355
Polar Surface Area
12.89
Rotatable Bonds
0
Lipinski's Rule of Five
true
Data Source
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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
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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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Synonyms
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IUPAC name
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IUPAC Traditional name
Registration numbers
Properties
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
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR42188
Sigma Aldrich
24098
TRC
C379980
Bide Pharmatech
BD7254
Academic Data
PubChem
69458
Names and Identifiers
Synonyms
5-Chloroquinoline
5-Chloroquinoline
5-氯喹啉
IUPAC name
5-chloroquinoline
IUPAC Traditional name
5-chloroquinoline
Registration numbers
PubChem CID
69458
PubChem SID
162075701
24854449
CAS Number
635-27-8
Beilstein Number
114722
MDL Number
MFCD00239413
Molecule Details
Sigma Aldrich
24098
Packaging
1 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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PubChem SID
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CAS Number
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Beilstein Number
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MDL Number
Properties
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Physical Property
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Safety Information
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Product Information
Properties
Physical Property
Melting Point
28-32°C
Source
28-32 °C
Source
Apperance
Yellow Solid
Source
Solubility
Ethyl Acetate
Source
Dichloromethane
Source
Safety Information
Storage Warning
Irritant/Keep Cold/Store under Argon
Source
36/37/38
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
Warning
Source
Irritant (Xi)
2-8°C
Source
Download link
Source
Download link
Source
dust mask type N95 (US), Eyeshields, Gloves
Source
3
Source
H315
-
H319
-
H335
Source
P261
-
P305+P351+P338
Source
26
-
36
Source
Product Information
C9H6ClN
Source
≥98.0% (GC)
Source
95+%
Source
Download link
Source
Source
Source
Risk Statements
GHS Pictograms
GHS Signal Word
European Hazard Symbols
Storage Temperature
MSDS Link
Personal Protective Equipment
German water hazard class
GHS Hazard statements
GHS Precautionary statements
Safety Statements
Empirical Formula (Hill Notation)
Purity
Certificate of Analysis