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6-Fluoronicotinic acid

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6-Fluoronicotinic acid Basic information

Product Name:
6-Fluoronicotinic acid
Synonyms:
  • 2-Fluoropyridine-5-carboxylic acid, 6-Fluoropyridine-3-carboxylic acid, 5-Carboxy-2-fluoropyridine, 3-Carboxy-6-fluoropyridine
  • 6-Floronicotinic acid
  • 6-Fluoronicotinc Acid
  • 2-Fluoropyridine-5-carboxylic acid, 6-Fluoropyridine-3-carboxylic acid, 5-Carboxy-2-fluoropyridine
  • 2-FLUOROPYRIDINE-5-CARBOXYLIC ACID
  • 2-FLUORO-5-PYRIDINE CARBOXYLIC ACID
  • 2-Fluoro-5-pyridine carboxylic acid(6-Fluoronicotinic acid)
  • 6-FLUORONICOTINIC ACID
CAS:
403-45-2
MF:
C6H4FNO2
MW:
141.1
EINECS:
251-228-4
Product Categories:
  • Chemical Synthesis
  • Fluorinated Building Blocks
  • Heterocyclic Building Blocks
  • Heterocyclic Fluorinated Building Blocks
  • Other Fluorinated Heterocycles
  • Picolinic acid series
  • Pyridine
  • Pyridine series
  • Pyridines
  • Building Blocks
  • Carboxy
  • Boronic Acid
  • API
  • C6
Mol File:
403-45-2.mol
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6-Fluoronicotinic acid Chemical Properties

Melting point:
144-148 °C(lit.)
Boiling point:
309.4±22.0 °C(Predicted)
Density 
1.419±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
powder to crystal
pka
3.41±0.10(Predicted)
color 
White to Orange to Green
InChI
InChI=1S/C6H4FNO2/c7-5-2-1-4(3-8-5)6(9)10/h1-3H,(H,9,10)
InChIKey
UJDLCTNVHJEBDG-UHFFFAOYSA-N
SMILES
C1=NC(F)=CC=C1C(O)=O
CAS DataBase Reference
403-45-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29333990

MSDS

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6-Fluoronicotinic acid Usage And Synthesis

Chemical Properties

White to Orange to Green powder to crystal.

Uses

6-Fluoronicotinic acid is a fluorinated nicotinic acid that is a derivative of pyridine, with a carboxylic acid at 3-position and a fluorine at 6-position. It is used as a pharmaceutical intermediate and a molecular scaffold to synthesize tracers for positron emission tomography, for visualizing and measuring changes in metabolic processes.

References

[1] LATIFA RBAH-VIDAL. Early detection and longitudinal monitoring of experimental primary and disseminated melanoma using [¹⁰F]ICF01006, a highly promising melanoma PET tracer.[J]. European Journal of Nuclear Medicine and Molecular Imaging, 2012, 39 9: 1449-1461. DOI:10.1007/s00259-012-2168-y.
[2] FALGUNI BASULI. Fast indirect fluorine-18 labeling of protein/peptide using the useful 6-fluoronicotinic acid-2,3,5,6-tetrafluorophenyl prosthetic group: A method comparable to direct fluorination.[J]. Journal of labelled compounds & radiopharmaceuticals, 2017, 60 3 1: 168-175. DOI:10.1002/jlcr.3487.
[3] G. F. HAWKINS ARTHUR R. THE PREPARATION OF 5-FLUORONICOTINIC ACID AND 5-FLUORONICOTINAMIDE1[J]. The Journal of Organic Chemistry, 1949, 14 2: 328-332. DOI:10.1021/jo01154a021.
[4] Lal, Achchhe, and Devendra Kumar Singh. "Theoretical and Experimental Studies of Vibrational Spectra of 6-fluoronicotinc Acid."

6-Fluoronicotinic acid Preparation Products And Raw materials

Raw materials

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