methyl 4-chloropyridine-3-carboxylate;hydrochloride|1351479-18-9,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 4-chloropyridine-3-carboxylate;hydrochloride

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Chemical Name:	methyl 4-chloropyridine-3-carboxylate;hydrochloride
CAS Number:	1351479-18-9
Product Number:	AG006ZD3(AGN-PC-0BHSEB)
Synonyms:
MDL No:
Molecular Formula:	C7H7Cl2NO2
Molecular Weight:	208.0420

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Chemical Structure

Methyl 4-chloronicotinate hydrochloride is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in the preparation of pharmaceuticals, agrochemicals, and various fine chemicals. Its unique structure allows for it to participate in a variety of reactions, making it a valuable tool for organic chemists. Additionally, the presence of the hydrochloride group enhances the compound's solubility and reactivity in a range of solvents, further expanding its utility in synthesis applications.