| Weight | 99.209 g/mol |
|---|---|
| Formula | C4H9NSi |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Trimethylsilyl cyanide (7677-24-9)
TMSCN
Score:
#7078 in Chemistry
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- Discovery of Chiral Catalysts through Ligand Diversity: TiCatalyzed Enantioselective Addition of TMSCN to meso Epoxides (Angewandte Chemie, 1996)
- THE ASYMMETRIC ADDITION OF TRIMETHYLSILYL CYANIDE TO ALDEHYDES CATALYZED BY CHIRAL (SALEN)TITANIUM COMPLEXES (Journal of the American Chemical Society, 1999)
- Synthetic applications of trimethylsilyl cyanide. Efficient synthesis of .beta.-aminomethyl alcohols (Journal of Organic Chemistry, 1974)
- Activation of TMSCN by N-Heterocyclic Carbenes for Facile Cyanosilylation of Carbonyl Compounds. (Journal of Organic Chemistry, 2006)
- Optimized catalysts for the asymmetric addition of trimethylsilyl cyanide to aldehydes and ketones (Tetrahedron, 2001)
- Asymmetric Ring Opening of Meso Epoxides with TMSCN Catalyzed by (pybox)lanthanide Complexes (Organic Letters, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - TMSCN
-
SMILESC[Si](C)(C)C#N
-
InChIKeyLEIMLDGFXIOXMT-UHFFFAOYSA-N
- Pubchem - Trimethylsilyl cyanide
- Wikipedia - Trimethylsilyl cyanide
Trimethylsilyl cyanide is the chemical compound with the formula (CH3)3SiCN. This volatile liquid consists of a cyanide group, that is CN, attached to a trimethylsilyl group. The molecule is used in organic synthesis as the equivalent of hydrogen cyanide.
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Chloro(chloromethyl)dimethylsilane
(1719-57-9)
2 alternate names
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Chlorodimethylvinylsilane
(1719-58-0)
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18156-15-5
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2083-91-2
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76513-69-4
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4-fluoro-1H-pyrazole
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7691-02-3
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Trimethylsilyl cyanide
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