1,4-Dibromo-2,3-bis(bromomethyl)but-2-ene

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Reagent Code: #171267
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CAS Number 30432-16-7

science Other reagents with same CAS 30432-16-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 399.74 g/mol
Formula C₆H₈Br₄
thermostat Physical Properties
Boiling Point 376.9°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a reactive intermediate in organic synthesis, this compound serves as a versatile cross-linking agent due to the presence of multiple bromomethyl groups. It is employed in the preparation of specialty polymers and functionalized hydrocarbons where controlled branching or network formation is required. Its high reactivity toward nucleophiles makes it suitable for quaternization reactions and the synthesis of complex molecular architectures, including cage-like structures and dendrimers. Additionally, it finds use in the development of flame retardants, where bromine content contributes to fire resistance in polymeric materials. Handling requires caution due to its lachrymatory and corrosive properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿143.00
inventory 1g
10-20 days ฿400.00
inventory 5g
10-20 days ฿1,930.00
inventory 25g
10-20 days ฿9,320.00

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1,4-Dibromo-2,3-bis(bromomethyl)but-2-ene
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Used primarily as a reactive intermediate in organic synthesis, this compound serves as a versatile cross-linking agent due to the presence of multiple bromomethyl groups. It is employed in the preparation of specialty polymers and functionalized hydrocarbons where controlled branching or network formation is required. Its high reactivity toward nucleophiles makes it suitable for quaternization reactions and the synthesis of complex molecular architectures, including cage-like structures and dendrimers.

Used primarily as a reactive intermediate in organic synthesis, this compound serves as a versatile cross-linking agent due to the presence of multiple bromomethyl groups. It is employed in the preparation of specialty polymers and functionalized hydrocarbons where controlled branching or network formation is required. Its high reactivity toward nucleophiles makes it suitable for quaternization reactions and the synthesis of complex molecular architectures, including cage-like structures and dendrimers. Additionally, it finds use in the development of flame retardants, where bromine content contributes to fire resistance in polymeric materials. Handling requires caution due to its lachrymatory and corrosive properties.

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