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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)-

6-fluoro-2-methoxypyridine-3-carbonitrile

COc1nc(F)ccc1C#N Request for Quotation
Chemical Name: 6-fluoro-2-methoxypyridine-3-carbonitrile
CAS Number: 1339175-72-2
Product Number: AG009WJT(AGN-PC-0JF43Q)
Synonyms:
MDL No:
Molecular Formula: C7H5FN2O
Molecular Weight: 152.1258

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Chemical Structure


6-Fluoro-2-methoxynicotinonitrile is a versatile compound commonly used in chemical synthesis as a key building block in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique molecular structure containing a fluorine atom and a methoxy group on a nicotinonitrile backbone, this compound serves as a valuable intermediate in the creation of various functionalized molecules.In organic synthesis, 6-Fluoro-2-methoxynicotinonitrile acts as a precursor for the preparation of diverse heterocyclic compounds through substitution, addition, or coupling reactions. Its fluorine substituent enhances the compound's reactivity and alters its electronic properties, making it particularly useful in designing bioactive molecules with improved pharmacological profiles.Furthermore, the methoxy group on the nicotinonitrile scaffold provides an opportunity for further modifications, allowing chemists to fine-tune the compound for specific applications. The presence of both electron-withdrawing and electron-donating groups in 6-Fluoro-2-methoxynicotinonitrile enables the control of regioselectivity and stereochemistry in complex chemical transformations.Overall, the strategic incorporation of 6-Fluoro-2-methoxynicotinonitrile in chemical synthesis enables the efficient construction of valuable intermediates and target molecules with potential utility in pharmaceutical research, agrochemical development, and materials science.