| Weight | 140.262 g/mol |
|---|---|
| Formula | C6H12N2Si |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
N-(Trimethylsilyl)imidazole (18156-74-6)
TSIM · 1-(trimethylsilyl)-1H-imidazole · N-trimethylsilylimidizole
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- Sigma-Aldrich - N-(Trimethylsilyl)imidazole20.60 - 353.00 USD
- Fisher Scientific - Search for N-(Trimethylsilyl)imidazole
- TCI - N-(Trimethylsilyl)imidazole42.00 - 193.00 USD
- A simple one-pot procedure for the direct conversion of alcohols into azides using TsIm (Tetrahedron Letters, 2007)
- One-pot synthesis of N-alkyl purine and pyrimidine derivatives from alcohols using TsIm: a rapid entry into carboacyclic nucleoside synthesis (Tetrahedron, 2008)
- The tsim tsoum approaches for prevention of cardiovascular disease. (Cardiology Research and Practice, 2010)
- Preparation of Monosilyl Acetals from Esters via iBu2AlH Reduction and Trapping with N-(Trimethylsilyl)imidazole. Addition of Allyltrimethylsilane To Yield Homoallylic Alcohols or Ethers (Journal of Organic Chemistry, 1995)
- A Simple OnePot Procedure for the Direct Conversion of Alcohols into Alkyl Nitriles Using TsIm. (Tetrahedron Letters, 2007)
- A simple procedure for the esterification of alcohols with sodium carboxylate salts using 1-tosylimidazole (TsIm) (Tetrahedron Letters, 2008)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - TSIM
- 1-(trimethylsilyl)-1H-imidazole
- N-trimethylsilylimidizole
- 1-trimethylsilylimidazole
- TMSIM
-
SMILESC[Si](C)(C)N1C=CN=C1
-
InChIKeyYKFRUJSEPGHZFJ-UHFFFAOYSA-N
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N-(Trimethylsilyl)imidazole
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