METHYL 2,6-DICHLORO-3-METHYLISONICOTINATE|125849-96-9,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)-

METHYL 2,6-DICHLORO-3-METHYLISONICOTINATE

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Chemical Name:	METHYL 2,6-DICHLORO-3-METHYLISONICOTINATE
CAS Number:	125849-96-9
Product Number:	AG000OUI(AGN-PC-0WAK1E)
Synonyms:
MDL No:
Molecular Formula:	C8H7Cl2NO2
Molecular Weight:	220.0527

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Chemical Structure

Methyl 2,6-dichloro-3-methylisonicotinate is a key intermediate in organic synthesis, commonly used in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique chemical structure makes it a versatile building block for creating complex molecules with specific properties and functions. In chemical synthesis, this compound serves as a valuable starting material for the preparation of various compounds through a series of chemical reactions such as nucleophilic substitution, condensation, and reduction. By incorporating Methyl 2,6-dichloro-3-methylisonicotinate into synthetic routes, chemists can efficiently access new compounds with diverse applications in various fields of chemistry.