tert-Butyl 3-methyl-3-(methylamino)piperidine-1-carboxylate|1420901-24-1,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)-

tert-Butyl 3-methyl-3-(methylamino)piperidine-1-carboxylate

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Chemical Name:	tert-Butyl 3-methyl-3-(methylamino)piperidine-1-carboxylate
CAS Number:	1420901-24-1
Product Number:	AG001HR7(AGN-PC-0WAH4M)
Synonyms:
MDL No:
Molecular Formula:	C12H24N2O2
Molecular Weight:	228.3312

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Chemical Structure

The tert-Butyl 3-methyl-3-(methylamino)piperidine-1-carboxylate is a versatile reagent commonly used in chemical synthesis for its unique properties. Its application in organic chemistry lies in its ability to serve as a building block in the production of various compounds. Due to its stable tert-butyl group and functional piperidine ring, this compound can participate in a wide range of reactions, leading to the formation of diverse products. In particular, it is frequently employed in the synthesis of pharmaceuticals, agrochemicals, and materials with complex structures. Its distinctive structure and reactivity make it a valuable tool for researchers and chemists seeking to create intricate molecules for various applications.