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Molecule
ID:66658
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₅H₄FNO
Molecular Mass
113.0897632
Exact Mass
113.02769197
Charge
0
InChI
InChI=1S/C5H4FNO/c6-5-2-1-4(8)3-7-5/h1-3,8H
InChIKey
HTRLNWYWOKWCLV-UHFFFAOYSA-N
Canonic Smiles
Fc1ccc(cn1)O
Isomeric Smiles
c1(ccc(cn1)O)F
Calculated Properties
JChem
Acid pKa
8.485691
H Acceptors
2
H Donor
1
LogD (pH = 5.5)
0.98820007
LogD (pH = 7.4)
0.95502144
Log P
0.98864067
Molar Refractivity
27.1131
Polarizability
9.792744
Polar Surface Area
33.12
Rotatable Bonds
0
Lipinski's Rule of Five
true
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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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Data Source
Commercial Catalog
Matrix Scientific
072069
Apollo Scientific
PC1240
Enamine
EN300-109417
Bide Pharmatech
BD21454
Alfa Aesar
H27741
A&J Pharmtech
AJA-O40356
Academic Data
PubChem
2763108
Names and Identifiers
Synonyms
2-Fluoro-5-hydroxypyridine
6-fluoropyridin-3-ol
2-Fluoro-5-hydroxypyridine
2-氟-5-羟基吡啶
6-Fluoro-3-pyridinol
2-Fluoro-5-hydroxypyridine 98%
IUPAC name
6-fluoropyridin-3-ol
IUPAC Traditional name
6-fluoropyridin-3-ol
Registration numbers
MDL Number
MFCD01075040
CAS Number
55758-32-2
PubChem SID
162032395
PubChem CID
2763108
Properties
Product Information
Purity
95+%
Source
95%
Source
98%
Source
Safety Information
TSCA Listed
false
Source
否
Source
Storage Warning
IRRITANT
Source
Irritant/Store under Argon/Keep Cold
Source
MSDS Link
Download link
Source
Safety Statements
26
-
37
Source
European Hazard Symbols
Irritant (Xi)
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
Risk Statements
36/37/38
Source
GHS Precautionary statements
P280G-
P305+P351+P338
Source
GHS Hazard statements
H315
-
H319
-
H335
Source
Physical Property
Melting Point
145-148°C
Source
150-153°C
Source
Hydrophobicity(logP)
1.204
Source
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay