2-Fluoro-6-(difluoromethoxy)pyridine|947534-62-5,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-

O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]

Tris(dibenzylideneacetone)dipalladium

C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C

Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-Fluoro-6-(difluoromethoxy)pyridine

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Chemical Name:	2-Fluoro-6-(difluoromethoxy)pyridine
CAS Number:	947534-62-5
Product Number:	AG00IIIL(AGN-PC-058CIV)
Synonyms:
MDL No:
Molecular Formula:	C6H4F3NO
Molecular Weight:	163.0973

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
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Identification/Properties

Computed Properties

Molecular Weight:

163.099g/mol

XLogP3:

2.5

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

163.024g/mol

Monoisotopic Mass:

163.024g/mol

Topological Polar Surface Area:

22.1A^2

Heavy Atom Count:

Formal Charge:

Complexity:

122

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

Signal Word:

Danger

UN#:

1993

Hazard Statements:

H226-H315-H319-H335

Precautionary Statements:

P261-P305+P351+P338

Class:

Packing Group:

Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure

2-(Difluoromethoxy)-6-fluoropyridine, also known by its chemical formula C6H3F3NO, is a powerful building block in chemical synthesis. With its unique combination of fluorine atoms and pyridine ring, this compound is highly versatile and widely used in the field of organic chemistry.One key application of 2-(Difluoromethoxy)-6-fluoropyridine is its role as a fluorinated heterocycle in drug discovery and development. Due to the presence of fluorine atoms, this compound can significantly influence the pharmacokinetic and pharmacodynamic properties of potential drug candidates. By incorporating 2-(Difluoromethoxy)-6-fluoropyridine into a molecule, medicinal chemists can modulate properties such as metabolic stability, bioavailability, and target selectivity.Additionally, 2-(Difluoromethoxy)-6-fluoropyridine is often employed as a synthetic intermediate in the preparation of complex organic molecules. Its reactivity and functional groups make it an ideal starting material for the construction of various pharmaceuticals, agrochemicals, and materials. Chemists can take advantage of the pyridine ring and fluorine substituents to introduce specific functionalities and stereochemistry in a controlled manner during the synthesis process.In summary, the use of 2-(Difluoromethoxy)-6-fluoropyridine in chemical synthesis offers a strategic approach to designing and accessing novel compounds with tailored properties for diverse applications in the fields of medicine, agriculture, and materials science.