추천 제품
Quality Level
분석
97%
양식
liquid
반응 적합성
reagent type: reductant
refractive index
n20/D 1.489 (lit.)
bp
73 °C/5 mmHg (lit.)
density
0.806 g/mL at 25 °C (lit.)
SMILES string
C[Si](C)(C)[SiH]([Si](C)(C)C)[Si](C)(C)C
InChI
1S/C9H28Si4/c1-11(2,3)10(12(4,5)6)13(7,8)9/h10H,1-9H3
InChI key
SQMFULTZZQBFBM-UHFFFAOYSA-N
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일반 설명
Tris(trimethylsilyl)silane is an organosilicon generally used as a radical reducing agent for xanthates, organic halides, isocyanides, selenides, and acid chlorides. It is also used for hydrosilylation of alkenes, alkynes, and dialkyl ketones.
애플리케이션
Super Silyl Protecting Groups
Used in:
Used in:
- Hydrosilylations
- Radical reactions
- Reductions of acid chlorides
- Reductions of carbon-halogen bonds
- Hydrosilations of carbonyls
- Another common application involves the use of the tris(trimethylsilyl)silyl (TTMSS, or super silyl) group when complexed with transition metals and main group elements
- More recently, the super silyl group is being utilized in carbon–carbon bond forming reactions
이미 열람한 고객
Accounts of Chemical Research, 25, 188-188 (1992)
Synlett, 91-91 (1990)
Tris (trimethylsilyl) silane: an efficient hydrosilylating agent of alkenes and alkynes
Kopping B, et al.
The Journal of Organic Chemistry, 57(14), 3994-4000 (1992)
Tris (trimethylsilyl) silane. A new reducing agent
Chatgilialoglu C, et al.
The Journal of Organic Chemistry, 53(15), 3641-3642 (1988)
Changxia Shi et al.
Science advances, 6(34), eabc0495-eabc0495 (2020-09-03)
Three types of seemingly unyielding trade-offs have continued to challenge the rational design for circular polymers with both high chemical recyclability and high-performance properties: depolymerizability/performance, crystallinity/ductility, and stereo-disorder/crystallinity. Here, we introduce a monomer design strategy based on a bridged bicyclic
문서
Explore methods for molecular monolayers on silicon surfaces, their properties, and applications in molecular electronics and sensing.
관련 콘텐츠
The Yamamoto group has employed several applications in catalysis.
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