2-(5,6-dimethoxypyridin-2-yl)ethanamine|1256825-11-2,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)-

2-(5,6-dimethoxypyridin-2-yl)ethanamine

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Chemical Name:	2-(5,6-dimethoxypyridin-2-yl)ethanamine
CAS Number:	1256825-11-2
Product Number:	AG000OH0(AGN-PC-0H6N77)
Synonyms:
MDL No:
Molecular Formula:	C9H14N2O2
Molecular Weight:	182.2197

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Chemical Structure

The compound 2-(5,6-Dimethoxypyridin-2-yl)ethanamine is a versatile building block in chemical synthesis. It serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. With its unique structure and reactivity, it can be used to introduce the pyridine ring into complex molecular structures, allowing for the modification of biological activity or physicochemical properties. Additionally, the amine functional group in this compound offers opportunities for further derivatization through various chemical reactions, enabling the creation of diverse molecular architectures for target-oriented synthesis.