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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
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-3-methoxypyridine

COc1cccnc1F Request for Quotation
Chemical Name: 2-fluoro-3-methoxypyridine
CAS Number: 163234-74-0
Product Number: AG001TXK(AGN-PC-07AAAD)
Synonyms:
MDL No:
Molecular Formula: C6H6FNO
Molecular Weight: 127.1163

Identification/Properties

Computed Properties
Molecular Weight:
127.118g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
127.043g/mol
Monoisotopic Mass:
127.043g/mol
Topological Polar Surface Area:
22.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
89.1
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Fluoro-3-methoxypyridine is a versatile chemical compound widely utilized in organic synthesis processes. This compound plays a crucial role in the development of various pharmaceuticals, agrochemicals, and materials due to its unique properties and reactivity.In chemical synthesis, 2-Fluoro-3-methoxypyridine serves as a valuable building block for the construction of complex molecules. Its fluoro substituent confers distinct stereochemical and electronic characteristics that can enhance the biological activity of the final products. This compound is frequently employed in the preparation of heterocyclic structures, which are prevalent in many bioactive compounds.Furthermore, the methoxy group present in the molecule can act as a directing group during synthetic transformations, facilitating regioselective reactions and enabling the introduction of additional functional groups at specific positions within the target molecule. This capability enhances the efficiency and precision of chemical synthesis processes, contributing to the synthesis of diverse compounds with tailored properties.Overall, 2-Fluoro-3-methoxypyridine is a valuable tool in the toolkit of synthetic chemists, enabling the construction of intricate molecular frameworks with applications across various industries, including pharmaceuticals, agrochemicals, and materials science.