2-Bromopropene, 99%, stab., Thermo Scientific Chemicals
2-Bromopropene, 99%, stab., Thermo Scientific Chemicals
Thermo Scientific Chemicals

2-Bromopropene, 99%, stab., Thermo Scientific Chemicals

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5 g
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100 g
Catalog number L14229.06
also known as L14229-06
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47.65
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Price (USD)/ Each
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Save 4.85 (9%)
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2-Bromopropene, 99%, stab., Thermo Scientific Chemicals
Catalog numberL14229.06
Price (USD)/ Each
47.65
Online exclusive
52.50 
Save 4.85 (9%)
-
Add to cart
Chemical Identifiers
CAS557-93-7
IUPAC Name2-bromoprop-1-ene
Molecular FormulaC3H5Br
InChI KeyPHMRPWPDDRGGGF-UHFFFAOYSA-N
SMILESCC(Br)=C
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SpecificationsSpecification SheetSpecification Sheet
Assay (GC)≥98.5% (UK sourced material)
CommentStabilised with Copper powder
Appearance (Color)Clear colorless to light yellow to pale brown
Assay from Supplier's CofA≥98.5% (GC, US sourced material)
Refractive Index1.4420-1.4460 @ 20?C (UK sourced material)
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2-Bromopropene is used as a solvent and as an intermediate for organic synthesis. It is also used as a fumigant. Further, it reacts with nonanal to prepare 2-methyl-undec-1-en-3-ol using chromium(II) chloride as a reagent. It is utilized as a refrigerant used in organic synthesis.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2-Bromopropene is used as a solvent and as an intermediate for organic synthesis. It is also used as a fumigant. Further, it reacts with nonanal to prepare 2-methyl-undec-1-en-3-ol using chromium(II) chloride as a reagent. It is utilized as a refrigerant used in organic synthesis.

Solubility
Immiscible with water.

Notes
Light sensitive. Incompatible with strong oxidizing agents and strong bases.
RUO – Research Use Only

General References:

  1. Bracco, L. L. B.; Badenes, M. P.; Tucceri, M. E.; Cobos, C. J. Theoretical kinetic study of the unimolecular decomposition of 2-bromopropene. Chem. Phys. Lett. 2014, 608, 386-392.
  2. Vila, C.; Giannerini, M.; Hornillos, V.; Fañanás-Mastral, M.; Feringa, B. L. Palladium-catalysed direct cross-coupling of secondary alkyllithium reagents. Chem. Sci. 2014, 5 (4), 1361-1367.