1,2,4,5-Tetrakis(bromomethyl)benzene

98%

Reagent Code: #242280
label
Alias Tetrabromotoluene; 1,2,4,5-tetrabromomethylbenzene
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CAS Number 15442-91-8

science Other reagents with same CAS 15442-91-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 449.80 g/mol
Formula C₁₀H₁₀Br₄
badge Registry Numbers
MDL Number MFCD00009664
thermostat Physical Properties
Melting Point 159-161 °C(lit.)
Boiling Point 326.93°C
inventory_2 Storage & Handling
Density 2.168 g/ml
Storage Room temperature, sealed

description Product Description

Used as a crosslinking agent in polymer chemistry, particularly in the synthesis of porous organic frameworks and covalent organic frameworks (COFs). Its four bromomethyl groups readily undergo nucleophilic substitution, enabling the formation of strong covalent bonds with amines, thiols, or other nucleophiles. This makes it valuable in constructing 3D network polymers for applications in gas storage, catalysis, and molecular separation. It is also employed in the preparation of functional resins and as a building block in supramolecular chemistry due to its rigid benzene core and multiple reactive sites.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,990.00
inventory 25g
10-20 days ฿11,230.00
inventory 100g
10-20 days ฿37,750.00

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1,2,4,5-Tetrakis(bromomethyl)benzene
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Used as a crosslinking agent in polymer chemistry, particularly in the synthesis of porous organic frameworks and covalent organic frameworks (COFs). Its four bromomethyl groups readily undergo nucleophilic substitution, enabling the formation of strong covalent bonds with amines, thiols, or other nucleophiles. This makes it valuable in constructing 3D network polymers for applications in gas storage, catalysis, and molecular separation. It is also employed in the preparation of functional resins and as

Used as a crosslinking agent in polymer chemistry, particularly in the synthesis of porous organic frameworks and covalent organic frameworks (COFs). Its four bromomethyl groups readily undergo nucleophilic substitution, enabling the formation of strong covalent bonds with amines, thiols, or other nucleophiles. This makes it valuable in constructing 3D network polymers for applications in gas storage, catalysis, and molecular separation. It is also employed in the preparation of functional resins and as a building block in supramolecular chemistry due to its rigid benzene core and multiple reactive sites.

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