[(5-bromopyridin-2-yl)methyl]dimethylamine|908271-69-2,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)-

[(5-bromopyridin-2-yl)methyl]dimethylamine

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Chemical Name:	[(5-bromopyridin-2-yl)methyl]dimethylamine
CAS Number:	908271-69-2
Product Number:	AG00IKYT(AGN-PC-0WAJA3)
Synonyms:
MDL No:
Molecular Formula:	C8H11BrN2
Molecular Weight:	215.0903

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Identification/Properties

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Chemical Structure

The compound [(5-bromopyridin-2-yl)methyl]dimethylamine, also known as $name$, is a versatile reagent widely utilized in chemical synthesis. Its unique structure containing both a pyridine ring and an amine group provides a foundation for a variety of reactions and transformations. In organic synthesis, $name$ is commonly employed as a nucleophilic catalyst, facilitating the formation of carbon-carbon, carbon-nitrogen, and carbon-oxygen bonds. Its ability to participate in diverse chemical reactions makes it a valuable building block for the creation of complex molecules and pharmaceutical intermediates. Additionally, $name$ can act as a chiral auxiliary, enabling the synthesis of enantiomerically pure compounds. Its compatibility with a range of reaction conditions and substrates makes it a versatile tool for synthetic chemists aiming to streamline the construction of novel molecular structures.