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Molecule
ID:7454
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/c8-7-3-6(9)2-1-5(7)4-10/h1-3H
InChIKey
PGKPNNMOFHNZJX-UHFFFAOYSA-N
Canonic Smiles
N#Cc1ccc(cc1Cl)F
Isomeric Smiles
C(#N)c1c(Cl)cc(F)cc1
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
13.78219
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
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
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Synonyms
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IUPAC name
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IUPAC Traditional name
Registration numbers
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Physical Property
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Product Information
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
PC1861L
Matrix Scientific
002497
Maybridge
TL00226
Sigma Aldrich
344265
Chemik
CHB31000
Enamine
EN300-66421
Bide Pharmatech
BD10189
Alfa Aesar
A15478
A&J Pharmtech
AJA-O2008
AJA-O5109
Academic Data
PubChem
109000
Names and Identifiers
Synonyms
2-Chloro-4-fluorobenzonitrile
2-Chloro-4-fluorobenzonitrile
2-氯-4-氟苯甲腈
2-Chloro-4-fluorobenzonitrile 99%
2-chloro-4-fluoro benzonitrile
IUPAC name
2-chloro-4-fluorobenzonitrile
IUPAC Traditional name
2-chloro-4-fluorobenzonitrile
Registration numbers
PubChem CID
109000
EC Number
262-384-8
CAS Number
60702-69-4
PubChem SID
160970761
24861237
MDL Number
MFCD00042523
Beilstein Number
6323034
Molecule Details
Sigma Aldrich
344265
Packaging
5 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
PubChem CID
•
EC Number
•
CAS Number
•
PubChem SID
•
MDL Number
•
Beilstein Number
Properties
Physical Property
Melting Point
63-65°C
Source
64-66 °C(lit.)
Source
64 - 66°C
Source
62-66°C
Source
Hydrophobicity(logP)
2.301
Source
Safety Information
TSCA Listed
false
Source
否
Source
Storage Warning
IRRITANT, IRRITANT-HARMFUL
Source
Toxic/Harmful
Source
MSDS Link
Download link
Source
Download link
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
GHS Hazard statements
H302
-
H312
-
H315
-
H319
-
H332
-
H335
Source
H311
-
H302
-
H332
-
H315
-
H319
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
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
GHS Signal Word
Warning
Source
European Hazard Symbols
Harmful (Xn)
Source
Harmful (X)
GHS Precautionary statements
P261
-
P280
-
P305+P351+P338
Source
P280H-
P305+P351+P338
-
P309
-
P310
Source
German water hazard class
3
Source
Risk Statements
20/21/22
-
36/37/38
Source
20/21/22
-
36/38
Source
Safety Statements
26
-
36
Source
26
-
36/37
Source
UN Number
UN3439
Source
Hazard Class
6.1
Source
Packing Group
III
Source
Product Information
Purity
99%
Source
97%
Source
95%
Source
98%
Source
Linear Formula
ClC6H3(F)CN
Source
Source
Source