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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)-

5-fluoro-6-methoxypyridine-2-sulfonyl chloride

COc1nc(ccc1F)S(=O)(=O)Cl Request for Quotation
Chemical Name: 5-fluoro-6-methoxypyridine-2-sulfonyl chloride
CAS Number: 1261783-55-4
Product Number: AG000S0B(AGN-PC-0AM1ND)
Synonyms:
MDL No:
Molecular Formula: C6H5ClFNO3S
Molecular Weight: 225.6252

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of 5-Fluoro-6-methoxypyridine-2-sulfonyl chloride in chemical synthesis lies in its versatile reactivity as a sulfonyl chloride derivative. This compound serves as a valuable building block in the creation of pharmaceuticals, agrochemicals, and other fine chemicals. By acting as a sulfonyl chloride, it can participate in numerous reactions such as substitution, addition, and coupling reactions to introduce the 5-fluoro-6-methoxypyridylsulfonyl moiety into target molecules. This functional group can impart desired properties or biological activities to the final products, making 5-Fluoro-6-methoxypyridine-2-sulfonyl chloride a key intermediate in the synthesis of complex organic compounds.