| Weight | 195.243 g/mol |
|---|---|
| Formula | C9H9NO2S |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Tosylmethyl isocyanide (36635-61-7)
TMIC isocyanide · 4-toluenesulfonylmethyl isocyanide · p-toluenesulphonylmethyl isocyanide
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- GENERAL ONE-STEP SYNTHESIS OF NITRILES FROM KETONES USING TOSYLMETHYL ISOCYANIDE - INTRODUCTION OF A ONE-CARBON UNIT (Journal of Organic Chemistry, 1977)
- THE ASYMMETRIC ALDOL REACTION OF TOSYLMETHYL ISOCYANIDE AND ALDEHYDES CATALYZED BY CHIRAL SILVER(I) COMPLEXES (Journal of Organic Chemistry, 1990)
- Novel synthesis of 4(5)-monosubstituted imidazoles via cycloaddition of tosylmethyl isocyanide to aldimines (Tetrahedron, 1997)
- Use of dilithio-tosylmethyl isocyanide in the synthesis of oxazoles and imidazoles (Tetrahedron Letters, 1980)
- Chemistry of sulfonylmethyl isocyanides. 45. A direct synthesis of 2-(trimethylstannyl)pyrroles from Michael acceptors and stannylated tosylmethyl isocyanide (Journal of Organic Chemistry, 1998)
- Tosylmethyl isocyanide employed in a novel synthesis of ketones. A new masked formaldehyde reagent (Tetrahedron Letters, 1977)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - TMIC isocyanide
- 4-toluenesulfonylmethyl isocyanide
- p-toluenesulphonylmethyl isocyanide
-
SMILESCC1=CC=C(C=C1)S(=O)(=O)C[N+]#[C-]
-
InChIKeyCFOAUYCPAUGDFF-UHFFFAOYSA-N
- Pubchem - Tosylmethyl isocyanide
- Wikipedia - tosylmethyl isocyanide
Toluenesulfonylmethyl isocyanide or TOSMIC is an organic compound with the formula CH3C6H4SO2CH2NC. The molecule contains both sulfonyl and isocyanide groups. It is a colourless solid that unlike many isocyanides, is odorless.
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Tosylmethyl isocyanide
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