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

ALDRICH/230995 - 96%

Synonym: 3-Bromopropionaldehyde ethylene acetal

CAS Number: 18742-02-4
Empirical Formula (Hill Notation): C5H9BrO2
Molecular Weight: 181.03
EC Number: 242-551-1
MDL Number: MFCD00003216
Linear Formula: C5H9BrO2
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-230995-10G 10 g
$72.10
1/EA
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45-230995-50G 50 g
$256.00
1/EA
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assay 96%
bp 68-70 °C/8 mmHg (lit.)
contains sodium bicarbonate as stabilizer
density 1.542 g/mL at 25 °C (lit.)
form liquid
InChI 1S/C5H9BrO2/c6-2-1-5-7-3-4-8-5/h5H,1-4H2
InChI key GGZQLTVZPOGLCC-UHFFFAOYSA-N
Quality Level 200 
refractive index n20/D 1.479 (lit.)
SMILES string BrCCC1OCCO1
storage temp. 2-8°C
Application: 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 pulo′upone via Evans′ asymmetric Diels-Alder reaction
• as alkylating agent for amines, dithianes and carboximides
• with eynamides and sodium azide in a "one-pot" synthesis of triazoles
General description: 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 is a cyclic ether derivative with a dioxolane ring, used as a building block in organic synthesis and polymer industry.
Packaging: 10, 50 g in glass bottle
Purity 96%
bp 68-70 °C/8 mmHg (lit.)
Density 1.542 g/mL at 25 °C (lit.)
Refractive Index n20/D 1.479 (lit.)
Storage Temp. 2-8°C
UNSPSC 12352100

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