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Sigma Aldrich 2-(2-Bromoethyl)-1,3-dioxolane
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- Copper-catalyzed borylation of 2-(2-bromoethyl)-1,3-dioxolane with bis(pinacolato)diboron followed by treatment with potassium bifluoride affords the key organotrifluoroborate reagent.2-(2-bromoethyl)-1,3-dioxolane was used:
- As starting reagent for the synthesis of (5z,9z)-5,9-hexadecadienoic acid, (5z,9z)-5,9-nonadecadienoic acid and (5z,9z)-5,9-eicosadienoic acid
- In synthesis of 1-deoxy-castanospermine and 1-deoxy-8a-epi-castanospermine
- In asymmetric total synthesis of both enantiomers of marine mollusk metabolite puloαupone via evansα asymmetric diels-alder reaction
- As alkylating agent for amines, dithianes and carboximides
- With eynamides and sodium azide in a one-pot synthesis of triazoles
Specifications
Specifications
| CAS | 18742-02-4 |
| Density | 1.542 g/mL (at 25°C (literature)) |
| Boiling Point | 68°C to 70°C (8 mmHg) |
| Molecular Formula | C5H9BrO2 |
| Refractive Index | n20/D 1.479 (literature) |
| Linear Formula | C5H9BrO2 |
| MDL Number | MFCD00003216 |
| Quantity | 50 g |
| Synonym | 3-Bromopropionaldehyde ethylene acetal |
| Molecular Weight (g/mol) | 181.03 |
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