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Molecule
ID:18447
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₆H₄FNO
Molecular Mass
125.1004632
Exact Mass
125.02769197
Charge
0
InChI
InChI=1S/C6H4FNO/c7-6-5(4-9)2-1-3-8-6/h1-4H
InChIKey
OFBVGDCXXGXDKU-UHFFFAOYSA-N
Canonic Smiles
O=Cc1cccnc1F
Isomeric Smiles
c1ccc(c(n1)F)C=O
Calculated Properties
JChem
H Acceptors
2
H Donor
0
LogD (pH = 5.5)
1.0047083
LogD (pH = 7.4)
1.0047083
Log P
1.0047083
Molar Refractivity
31.7162
Polarizability
11.069602
Polar Surface Area
29.96
Rotatable Bonds
1
Lipinski's Rule of Five
true
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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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Bioactivity
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General Information
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RDKit
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Names and Identifiers
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IUPAC name
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Synonyms
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IUPAC Traditional name
Registration numbers
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MDL Number
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PubChem SID
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CAS Number
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PubChem CID
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Product Information
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Safety Information
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Physical Property
Related Proteins
Molecular Spectra
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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
PC7036
Matrix Scientific
020578
Sigma Aldrich
664111
Bide Pharmatech
BD28504
A&J Pharmtech
AJA-O34581
Academic Data
PubChem
11434944
Names and Identifiers
IUPAC name
2-fluoropyridine-3-carbaldehyde
Synonyms
2-Fluoropyridine-3-carbaldehyde
2-Fluoropyridine-3-carboxaldehyde
2-氟-3-甲酰基吡啶
2-Fluoronicotinaldehyde
2-氟烟醛
2-Fluoro-3-formylpyridine
2-Fluoro-3-pyridinecarboxaldehyde
2-Fluoro-3-formylpyridine
IUPAC Traditional name
2-fluoropyridine-3-carbaldehyde
Registration numbers
MDL Number
MFCD03095270
PubChem SID
24884681
160981754
CAS Number
36404-90-7
PubChem CID
11434944
Molecule Details
Sigma Aldrich
664111
Application
Attachment of isoxazolinones by displacement of fluoride provide naphthyridines on hydrogenolysis and cyclization.1
Packaging
5 g in glass bottle
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay
Properties
Product Information
Purity
97%
Source
98%
Source
Empirical Formula (Hill Notation)
C6H4FNO
Source
Safety Information
TSCA Listed
false
Source
MSDS Link
Download link
Source
Download link
Source
Storage Warning
IRRITANT
Source
Harmful/Irritant
Source
Safety Statements
26
Source
German water hazard class
3
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
GHS Hazard statements
H302
-
H315
-
H319
-
H335
Source
European Hazard Symbols
Harmful (Xn)
Source
Personal Protective Equipment
Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
Risk Statements
36/37/38
Source
GHS Signal Word
Warning
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
Physical Property
Density
1.250
Source
1.250 g/mL at 25 °C
Source
Flash Point
73°C
Source
163.4 °F
Source
73 °C
Source
Boiling Point
50°C
Source
50 °C/3 mmHg
Source
n20/D 1.520
Source
Refractive Index