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Molecule
ID:7665
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₃ClFN
Molecular Mass
155.5568232
Exact Mass
154.993805
Charge
0
InChI
InChI=1S/C7H3ClFN/c8-6-2-1-3-7(9)5(6)4-10/h1-3H
InChIKey
XPTAYRHLHAFUOS-UHFFFAOYSA-N
Canonic Smiles
N#Cc1c(F)cccc1Cl
Isomeric Smiles
Fc1c(c(Cl)ccc1)C#N
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
2.5760887
LogD (pH = 7.4)
2.5760887
Log P
2.5760887
Molar Refractivity
36.8008
Polarizability
13.783144
Polar Surface Area
23.79
Rotatable Bonds
0
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
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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
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Properties
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Product Information
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Physical Property
Related Proteins
Molecular Spectra
Molecule Details
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Apollo Scientific
•
Sigma Aldrich
References
•
PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
PC1863
Matrix Scientific
002771
Sigma Aldrich
188182
24625
Chemik
CHB30800
Bide Pharmatech
BD10191
Alfa Aesar
B21662
Academic Data
PubChem
69587
Registration numbers
CAS Number
668-45-1
MDL Number
MFCD00001780
PubChem CID
69587
PubChem SID
160970972
24851304
Beilstein Number
1940332
EC Number
211-571-2
Molecule Details
Apollo Scientific
PC1863
Treatment with nucleophiles e.g alkoxides can selectively displace the fluorine atom: Synth. Commun., 621 (1984)
Sigma Aldrich
188182
Packaging
10 g in glass bottle
References
PubChem Literature
From Data Sources
•
The fluorine atom can be selectively displaced by nucleophiles, e.g. alkoxides:
Synth. Commun
.,
14
, 621 (1984).
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
PubChem CID
•
PubChem SID
•
Beilstein Number
•
EC Number
Properties
Safety Information
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Download link
Source
IRRITANT
Source
Toxic
Source
P261
-
P280
-
P305+P351+P338
Source
P280H-
P305+P351+P338
-
P309
-
P310
Source
dust mask type N95 (US), Eyeshields, Gloves
Source
3439
Source
UN3439
Source
3
Source
III
Source
3
Source
H302
-
H312
-
H315
-
H319
-
H332
-
H335
Source
H311
-
H302
-
H332
-
H315
-
H319
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
20/21/22
-
36/37/38
Source
20/21/22
-
36/38
Source
26
-
37/39
Source
26
-
36/37
Source
6.1
Source
UN 3439 6.1/PG 3
Source
Harmful (Xn)
Product Information
98%
Source
≥98.0% (GC)
Source
ClC6H3(F)CN
Source
purum
Source
Physical Property
56-59°C
Source
55-59 °C(lit.)
Source
55-59 °C
Source
56-60°C
Source
104°C/11mm
Source
104 °C/11 mmHg(lit.)
Source
104-105°C/11mm
Source
Source
Source
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Source
Source
Harmful (X)
Source
Storage Warning
GHS Precautionary statements
Personal Protective Equipment
UN Number
Packing Group
German water hazard class
GHS Hazard statements
GHS Pictograms
GHS Signal Word
Risk Statements
Safety Statements
Hazard Class
RID/ADR
European Hazard Symbols
Purity
Linear Formula
Grade
Melting Point
Boiling Point
Names and Identifiers
IUPAC Traditional name
2-chloro-6-fluorobenzonitrile
IUPAC name
2-chloro-6-fluorobenzonitrile
Synonyms
2-Chloro-6-fluorobenzonitrile
2-氯-6-氟苯甲腈
2-Chloro-6-fluorobenzonitrile
2-Chloro-6-fluorobenzonitrile 98%
Names and Identifiers
•
IUPAC Traditional name
•
IUPAC name
•
Synonyms