|
| | 1-(TRIISOPROPYLSILYL)PYRROLE Basic information |
| | 1-(TRIISOPROPYLSILYL)PYRROLE Chemical Properties |
| Boiling point | 78 °C0.4 mm Hg(lit.) | | density | 0.904 g/mL at 25 °C(lit.) | | refractive index | n20/D 1.492(lit.) | | Fp | 224 °F | | storage temp. | Inert atmosphere,2-8°C | | pka | -2.55±0.70(Predicted) | | form | clear liquid | | color | Colorless to Almost colorless | | Specific Gravity | 0.904 | | Water Solubility | Not miscible in water. | | Sensitive | Moisture Sensitive | | Hydrolytic Sensitivity | 7: reacts slowly with moisture/water | | BRN | 3540663 | | CAS DataBase Reference | 87630-35-1(CAS DataBase Reference) |
| Hazard Codes | Xn | | Risk Statements | 20-22-36 | | Safety Statements | 24/25-26 | | WGK Germany | 3 | | HS Code | 2933998090 |
| | 1-(TRIISOPROPYLSILYL)PYRROLE Usage And Synthesis |
| Uses | 1-(Triisopropylsilyl)pyrrole may be employed as reagent in perfluoroalkylation and Vilsmeier formylation reactions. It may be used in the preparation of ethyl 2-(2,4-dinitrophenylhydrazono]-3-[ 1-(triisopropylsily1)-pyrrol-2-yflpropanoate; heterocyclic base, 3-nitropyrrole and 3-nitropyrrole, required for the synthesis of 1 -(2?-deoxy-β-D-ribofuranosyl)-3-nitropyrrole. It participates in various electrophilic substitution reactions specifically at β-position, via reaction with various electrophilic reagents (Br+, I+,NO2+,etc). | | Uses | 1-(Triisopropylsilyl)pyrrole may be employed as reagent in perfluoroalkylation and Vilsmeier formylation reactions. It may be used in the preparation of:
- ethyl 2-(2,4-dinitrophenylhydrazono]-3-[ 1-(triisopropylsily1)-pyrrol-2-yflpropanoate
- heterocyclic base, 3-nitropyrrole
- 3-nitropyrrole, required for the synthesis of 1 -(2′-deoxy-β-D-ribofuranosyl)-3-nitropyrrole
| | General Description | 1-(Triisopropylsilyl)pyrrole (TISP), a heterocyclic building block, is a pyrrole derivative. TISP has been reported to generate pyrrolic cation radicals during cyclovoltammetric studies, via electroreduction. It participates in various electrophilic substitution reactions specifically at β-position, via reaction with various electrophilic reagents (Br+, I+,NO2+,etc). |
| | 1-(TRIISOPROPYLSILYL)PYRROLE Preparation Products And Raw materials |
|