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Sigma Aldrich 2-(2-Bromoethyl)-1,3-dioxolane

Catalog No. 23099550G Shop All MilliporeSigma Sigma Organic Chemistry Products
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23-099-550G 50 g
23-099-510G 10 g
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MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.

  • 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

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
Percent Purity 96%
Biological Activity Respiratory System
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