N-烯丙基-N,N-双(三甲基甲硅烷基)胺，N-Allyl-N,N-bis(trimethylsilyl)amine；97%

N-Allyl-N,N-bis(trimethylsilyl)amine or N,N-bis(trimethylsilyl)prop-2-en-1-amine (AHMDS) can be used as a nucleophilic reagent to prepare:

• Complex bicyclic scaffolds by reacting with aryl aldehydes via imine formation followed by efficient multicomponent reactions.[1]
• Dithiasuccinoyl (Dts) heterocycle by reacting with bisthiocarbamoyl chloride.[1]
• Allyl selenide by reacting with aryl selenium salt in the presence of a ruthenium catalyst; Allyl selenide is utilized as a key intermediate in organic synthesis.[1]

AHMDS can also be used as a reagent in hydrosilylation and hydroboration reaction.[1] It may be also used as an electrolyte additive.[2]