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| | Heptyltriphenylphosphonium bromide Basic information |
| | Heptyltriphenylphosphonium bromide Chemical Properties |
| Melting point | 173-176 °C(lit.) | | storage temp. | Inert atmosphere,Room Temperature | | solubility | almost transparency in Methanol | | form | Fine Crystalline Powder | | color | White | | Sensitive | Hygroscopic | | BRN | 3580843 | | CAS DataBase Reference | 13423-48-8(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36-37 | | WGK Germany | 3 | | HS Code | 29319000 |
| | Heptyltriphenylphosphonium bromide Usage And Synthesis |
| Chemical Properties | white fine crystalline powder | | Uses | Reactant for:
- Stereospecific rearrangement of epoxides to quaternary carbaldehydes
- Synthesis of the male pheromone of two species of termite Zootermopsis
- Regio- and stereoselective TEMPO oxidation
- Diastereoselective synthesis of climacostol for antitumor activity
- Enantioselective synthesis of chiral vinylphosphonate and phosphonate analogs of immunosuppressive agent FTY720
- Preparation of embelin derivatives with XIAP inhibitory and anticancer activity
| | Uses | Heptyltriphenylphosphonium Bromide can be used for next Reaction:
- Stereospecific rearrangement of epoxides to quaternary carbaldehydes.
- Synthesis of the male pheromone of two species of termite Zootermopsis.
- Regio- and stereoselective TEMPO oxidation.
- Diastereoselective synthesis of climacostol for antitumor activity.
- Enantioselective synthesis of chiral vinylphosphonate and phosphonate analogs of immunosuppressive agent FTY720.
- Preparation of embelin derivatives with XIAP inhibitory and anticancer activity.
| | reaction suitability | reaction type: C-C Bond Formation |
| | Heptyltriphenylphosphonium bromide Preparation Products And Raw materials |
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