Catalog Number | ACM1873774-1 |
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CAS Number | 1873-77-4 |
Structure | ![]() |
Synonyms | 1,1,1,3,3,3-Hexamethyl-2-(trimethylsilyl)trisilane; TTMSS |
Molecular Weight | 248.66 g/mol |
Molecular Formula | C9H28Si4 |
Flash Point | 55 °C |
Purity | >90% |
Appearance | Colorless to Light yellow clear liquid |
Application | Tris(trimethylsilyl)silane serves as a versatile organosilicon compound with a range of applications in synthetic chemistry Primarily it functions as a radical-based reducing agent effectively engaging in reactions involving organic halides selenides xanthates isocyanides and ketones often delivering high yields It offers an alternative to tri-n-butylstannane in radical reactions due to its nontoxic nature and unique ability to provide complementary stereoselectivity particularly in the reduction of gem dihalides As a mild reducing reagent it is involved in nucleoside chemistry Additionally it plays a role in hydrosilylation processes with alkenes alkynes and dialkyl ketones and contributes to the synthesis of silated alkenes alkynes and fused quinolines Tris(trimethylsilyl)silane is also known for forming complexes with both transition metals and main group elements further broadening its utility in facilitating carbon-carbon bond-forming reactions It's noteworthy for its exothermic decomposition above 100 °C which should be considered during its application in various synthetic transformations |
Storage | Store under inert gas |
MDL Number | MFCD00077893 |
Reaxys Registry Number | 1923953 |
Specific Gravity | 0.81 |
Excellent Reducing Agent for Radical Reactions
I've used Alfa Chemistry's Tris(Trimethylsilyl)Silane in our lab for hydrosilylation of carbonyls. It's a non-toxic, effective substitute for tri-n-butylstannane in radical reactions, delivering high yields consistently. Highly recommended for organic synthesis!
※ Please kindly noted that this product is for research use only.