Weight | 175.518 g/mol |
---|---|
Formula | C3H5Cl3Si |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
ALLYLTRICHLOROSILANE (107-37-9)
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- Chiral 2,2-Bipyridine-Type N-Monoxides as Organocatalysts in the Enantioselective Allylation of Aldehydes with Allyltrichlorosilane (Organic Letters, 2002)
- Asymmetric allylation of aldehydes with allyltrichlorosilane promoted by chiral sulfoxides (Tetrahedron Letters, 2003)
- Chiral pyridine N-oxides derived from monoterpenes as organocatalysts for stereoselective reactions with allyltrichlorosilane and tetrachlorosilane (Tetrahedron, 2008)
- Additive effects on ligand activated allylation of aldehydes by allyltrichlorosilane (Tetrahedron Letters, 1997)
- Chiral Biscarboline N,NDioxide Derivatives: Highly Enantioselective Addition of Allyltrichlorosilane to Aldehydes (Advanced Synthesis & Catalysis, 2012)
- Asymmetric Allylation of Aldehydes with Allyltrichlorosilane Using Aza-paracyclophane-oxazoline-N-oxide Catalysts. (Tetrahedron Letters, 2006)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC=CC[Si](Cl)(Cl)Cl
-
InChIKeyHKFSBKQQYCMCKO-UHFFFAOYSA-N
- Pubchem - ALLYLTRICHLOROSILANE
- Wikipedia - allyltrichlorosilane
Allyltrichlorosilane is an organosilicon compound with the formula Cl3SiCH2CH=CH2. It is a colorless or white low-melting solid. It was originally prepared by the Direct process, the reaction of allyl chloride with copper-silicon alloy.
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