CAS 7688-51-9 N,N-Bis(Trimethylsilyl)Allylamine

NAVIGATION

N,N-Bis(Trimethylsilyl)Allylamine

PRICE INQUIRY

Catalog Number

ACM7688519-2

CAS Number

7688-51-9

Product Name

N,N-Bis(Trimethylsilyl)Allylamine

Structure

Category

Salt

Synonyms

578932_ALDRICH, EINECS 231-699-2, MolPort-003-937-319, N,N-Bis(trimethylsilyl)allylamine, CID82125, N-Allyl-N,N-bis(trimethylsilyl)amine, N-Allyl-1,1,1-trimethyl-N-(trimethylsilyl)silylamine, Silanamine, 1,1,1-trimethyl-N-2-propenyl-N-(trimethylsilyl)-, 7688-51-9

IUPAC Name

N,N-bis(trimethylsilyl)prop-2-en-1-amine

Molecular Weight

201.46 g/mol

Molecular Formula

C9H23NSi2

Canonical SMILES

C[Si](C)(C)N(CC=C)[Si](C)(C)C

InChI Key

CVNCFZIIZGNVFD-UHFFFAOYSA-N

Boiling Point

72ºC15 mm Hg(lit.)

Flash Point

109 °F

Purity

95%+

Density

0.816 g/mL at 25ºC(lit.)

Appearance

Transparent liquid

Application

N,N-Bis(Trimethylsilyl)Allylamine serves as a versatile nucleophilic reagent in organic synthesis. It enables the construction of complex bicyclic scaffolds through reactions with aryl aldehydes via imine formation, followed by efficient multicomponent reactions. Additionally, it can react with bisthiocarbamoyl chloride to form dithiasuccinoyl heterocycles, and with aryl selenium salts in the presence of a ruthenium catalyst to produce allyl selenide. The latter is particularly valuable as a key intermediate in various organic synthesis processes. Beyond these applications, N,N-Bis(Trimethylsilyl)Allylamine is also employed in hydrosilylation and hydroboration reactions and may serve as an additive in electrolytes.

EC Number

231-699-2

Exact Mass

201.13700

Hazard Statements

Packaging

10 g; 100 g;

Safety Description

16-26-36/37

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