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Molecule
ID:7677
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₇H₃FIN
Molecular Mass
247.0082932
Exact Mass
246.92942532
Charge
0
InChI
InChI=1S/C7H3FIN/c8-6-2-1-3-7(9)5(6)4-10/h1-3H
InChIKey
FAACTMVXBNSPJA-UHFFFAOYSA-N
Canonic Smiles
N#Cc1c(F)cccc1I
Isomeric Smiles
C(#N)c1c(F)cccc1I
Calculated Properties
JChem
H Acceptors
1
H Donor
0
LogD (pH = 5.5)
2.9009883
LogD (pH = 7.4)
2.9009883
Log P
2.9009883
Molar Refractivity
45.3585
Polarizability
17.202974
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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Academic Data
Names and Identifiers
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Synonyms
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IUPAC name
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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
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PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
PC3784
Matrix Scientific
002786
Sigma Aldrich
519359
Chemik
CHB32000
Enamine
EN300-67480
Bide Pharmatech
BD10222
Alfa Aesar
A11576
A&J Pharmtech
AJA-O38486
Academic Data
PubChem
522722
Names and Identifiers
Synonyms
2-Fluoro-6-iodobenzonitrile
2-氟-6-碘苯甲腈
2-Fluoro-6-iodobenzonitrile
2-Fluoro-6-iodobenzonitrile 98%
IUPAC name
2-fluoro-6-iodobenzonitrile
IUPAC Traditional name
2-fluoro-6-iodobenzonitrile
Registration numbers
PubChem SID
160970984
24874076
PubChem CID
522722
CAS Number
79544-29-9
MDL Number
MFCD00015478
Beilstein Number
4971873
Molecule Details
Sigma Aldrich
519359
Packaging
1, 5 g in glass bottle
References
PubChem Literature
No Data Available
Click here to submit data
Bioactivity
PubChem BioAssay
Registration numbers
•
PubChem SID
•
PubChem CID
•
CAS Number
•
MDL Number
•
Beilstein Number
Properties
Safety Information
MSDS Link
Download link
Source
Download link
Source
TSCA Listed
false
Source
否
Source
Storage Warning
IRRITANT, LIGHT SENSITIVE, IRRITANT-HARMFUL, TOXIC
Source
Toxic/Harmful/Irritant/Light Sensitive/Keep Cold
Source
Light Sensitive
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
GHS Hazard statements
H302
-
H312
-
H332
Source
H331
-
H302
-
H312
-
H315
-
H319
-
H335
Source
European Hazard Symbols
Harmful (Xn)
Source
Harmful (X)
GHS Precautionary statements
P280
Source
P261
-
P305+P351+P338
-
P302+P352
-
P321
-
P405
-P501A
Source
Safety Statements
36/37
Source
9
-
26
-
36/37
Source
Risk Statements
20/21/22
Source
20/21/22
-
36/37/38
Source
German water hazard class
3
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
UN Number
UN3439
Source
Hazard Class
6.1
Source
Packing Group
III
Source
Physical Property
Melting Point
49-51°C
Source
48-53°C
Source
49-53 °C(lit.)
Source
50 - 52°C
Source
48-52°C
Source
Hydrophobicity(logP)
2.841
Source
Product Information
Purity
98%
Source
97%
Source
95%
Source
Linear Formula
FC6H3(I)CN
Source
Source
Source