Bromocyclopentane, 98+%
Bromocyclopentane, 98+%
Bromocyclopentane, 98+%
Bromocyclopentane, 98+%
Thermo Scientific Chemicals

Bromocyclopentane, 98+%

CAS: 137-43-9 | C5H9Br | 149.031 g/mol
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Catalog NumberQuantity
ALFA15455.22100 g
Catalog number ALFA15455.22
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Quantity:
100 g
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Specifications
Chemical Name or MaterialBromocyclopentane
CAS137-43-9
Health Hazard 1H226
Health Hazard 2GHS H Statement
H226
Health Hazard 3P210-P233-P240-P241-P242-P243-P280-P303+P361+P353-P370+P378q-P501c
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Bromocyclopentane is a precursor used in the preparation of cyclopentene and cyclopentanol. It is a fatty bromide, which is used as a solvent. It is used as an intermediate for the preparation of surfactant and pharmaceuticals and other organic compounds.

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
Bromocyclopentane is a precursor used in the preparation of cyclopentene and cyclopentanol. It is a fatty bromide, which is used as a solvent. It is used as an intermediate for the preparation of surfactant and pharmaceuticals and other organic compounds.

Solubility
Immiscible with water.

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

General References:

  1. Sawant, D. K.; Klaassen, J. J.; Gounev, T. K.; Durig, J. R. r0 Structural parameters, conformational, vibrational studies and ab initio calculations of cyanocyclopentane. Spectrochim. Acta, Part A 2015, 151, 468-479.
  2. Paju, A.; Kostomarova, D.; Matkevitš, K.; Laos, M.; Pehk, T.; Kanger, T.; Lopp, M. 3-Alkyl-1,2-cyclopentanediones by Negishi cross-coupling of a 3-bromo-1,2-cyclopentanedione silyl enol ether with alkylzinc reagents: an approach to 2-substituted carboxylic acid gamma-lactones, homocitric and lycoperdic acids. Tetrahedron 2015, 71 (49), 9313-9320.