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Molecule
ID:18844
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₈H₆FN
Molecular Mass
135.1383432
Exact Mass
135.04842742
Charge
0
InChI
InChI=1S/C8H6FN/c1-6-2-3-8(9)4-7(6)5-10/h2-4H,1H3
InChIKey
IBRODYNXELBTJC-UHFFFAOYSA-N
Canonic Smiles
N#Cc1cc(F)ccc1C
Isomeric Smiles
C(#N)c1c(C)ccc(F)c1
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
2.4854653
LogD (pH = 7.4)
2.4854653
Log P
2.4854653
Molar Refractivity
37.0372
Polarizability
13.584135
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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RDKit
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JChem
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IUPAC name
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Synonyms
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IUPAC Traditional name
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Safety Information
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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
PC3823C
Matrix Scientific
021043
Sigma Aldrich
364916
Chemik
CHB32600
Enamine
EN300-62619
Alfa Aesar
A13061
Bide Pharmatech
BD10978
Academic Data
PubChem
522668
Names and Identifiers
IUPAC name
5-fluoro-2-methylbenzonitrile
Synonyms
5-Fluoro-2-methylbenzonitrile
5-氟-2-甲基苯甲腈
5-Fluoro-2-methylbenzonitrile
5-Fluoro-o-tolunitrile
5-Fluoro-2-methylbenzonitrile 98%
2-Cyano-4-fluorotoluene
5-氟-2-甲基苯腈
IUPAC Traditional name
5-fluoro-2-methylbenzonitrile
Registration numbers
Beilstein Number
7700578
MDL Number
MFCD00042295
CAS Number
77532-79-7
PubChem SID
24862466
160982151
PubChem CID
522668
Molecule Details
Sigma Aldrich
364916
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
Beilstein Number
•
MDL Number
•
CAS Number
•
PubChem SID
•
PubChem CID
Properties
Safety Information
TSCA Listed
false
Source
否
Source
MSDS Link
Download link
Source
Download link
Source
Storage Warning
TOXIC
Source
Irritant
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
H315
-
H318
-
H335
Source
H331
-
H302
-
H312
-
H315
-
H319
-
H335
Source
37/38
-
41
Source
20/21/22
-
36/37/38
Source
3
Source
P261
-
P280
-
P305+P351+P338
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Danger
Source
Irritant (Xi)
26
-
39
Source
9
-
26
-
36/37
Source
6.1
Source
UN3439
Source
III
Source
Physical Property
42-44°C
Source
43-45 °C(lit.)
Source
42-44°C
Source
79°C
Source
174.2 °F
Source
79 °C
Source
79°C(174°F)
Source
Product Information
98%
Source
95%
Source
FC6H3(CH3)CN
Source
Source
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Source
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Source
Source
Harmful (X)
Source
2.357
Source
GHS Pictograms
Personal Protective Equipment
GHS Hazard statements
Risk Statements
German water hazard class
GHS Precautionary statements
GHS Signal Word
European Hazard Symbols
Safety Statements
Hazard Class
UN Number
Packing Group
Melting Point
Flash Point
Hydrophobicity(logP)
Purity
Linear Formula