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

2-Bromopropene, 99%, stab.

CAS: 557-93-7 | C3H5Br | 120.977 g/mol
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数量:
5 g
25 g
100 g
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製品番号（カタログ番号） L14229.06
または、製品番号L14229-06
価格（JPY）
-
数量:
5 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS557-93-7
IUPAC Name2-bromoprop-1-ene
Molecular FormulaC3H5Br
InChI KeyPHMRPWPDDRGGGF-UHFFFAOYSA-N
SMILESCC(Br)=C
さらに表示
仕様Specification Sheetスペックシート
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)
さらに表示
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.