5-Bromohex-1-ene

95%

Reagent Code: #153363
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CAS Number 4558-27-4

science Other reagents with same CAS 4558-27-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.06 g/mol
Formula C₆H₁₁Br
badge Registry Numbers
MDL Number MFCD00049141
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the construction of complex molecules through its reactive alkene and bromine functionalities. The terminal double bond allows for polymerization or addition reactions, while the bromine atom enables cross-coupling reactions such as Suzuki or Heck couplings. It is also employed in the preparation of pharmaceuticals, agrochemicals, and specialty monomers for functional polymers. Its bifunctional nature makes it valuable for building carbon chains with specific branching or functional group placement.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,980.00
inventory 250mg
10-20 days ฿16,510.00
inventory 1g
10-20 days ฿50,630.00

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5-Bromohex-1-ene
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Used primarily as an intermediate in organic synthesis, this compound serves in the construction of complex molecules through its reactive alkene and bromine functionalities. The terminal double bond allows for polymerization or addition reactions, while the bromine atom enables cross-coupling reactions such as Suzuki or Heck couplings. It is also employed in the preparation of pharmaceuticals, agrochemicals, and specialty monomers for functional polymers. Its bifunctional nature makes it valuable for bu

Used primarily as an intermediate in organic synthesis, this compound serves in the construction of complex molecules through its reactive alkene and bromine functionalities. The terminal double bond allows for polymerization or addition reactions, while the bromine atom enables cross-coupling reactions such as Suzuki or Heck couplings. It is also employed in the preparation of pharmaceuticals, agrochemicals, and specialty monomers for functional polymers. Its bifunctional nature makes it valuable for building carbon chains with specific branching or functional group placement.

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