Aluminium bromide

98%

Reagent Code: #134660
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Alias Aluminum bromide; Aluminum tribromide
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CAS Number 7727-15-3
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Properties Sensitive to humidity

science Other reagents with same CAS 7727-15-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.69 g/mol
Formula AlBr₃
badge Registry Numbers
EC Number 231-779-7
MDL Number MFCD00003421
thermostat Physical Properties
Melting Point 94-98 °C(lit.)
Boiling Point 265 °C
inventory_2 Storage & Handling
Density 3.205 g/mL at 25 °C(lit.)
Storage 2~8 ℃, dry, inert gas atmosphere

description Product Description

Aluminium bromide is widely used as a catalyst in organic synthesis, particularly in reactions such as alkylation and acylation of aromatic compounds. It plays a key role in Friedel-Crafts reactions, where it helps form carbon-carbon bonds by activating alkyl or acyl halides. Its strong Lewis acidity makes it effective in promoting electrophilic substitution processes. It is also employed in the production of other brominated compounds and in certain polymerization reactions. Due to its reactivity with moisture, it is typically handled under anhydrous conditions in industrial and laboratory settings.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,330.00
inventory 25g
10-20 days ฿5,390.00
inventory 100g
10-20 days ฿20,190.00

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Aluminium bromide
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Aluminium bromide is widely used as a catalyst in organic synthesis, particularly in reactions such as alkylation and acylation of aromatic compounds. It plays a key role in Friedel-Crafts reactions, where it helps form carbon-carbon bonds by activating alkyl or acyl halides. Its strong Lewis acidity makes it effective in promoting electrophilic substitution processes. It is also employed in the production of other brominated compounds and in certain polymerization reactions. Due to its reactivity with m

Aluminium bromide is widely used as a catalyst in organic synthesis, particularly in reactions such as alkylation and acylation of aromatic compounds. It plays a key role in Friedel-Crafts reactions, where it helps form carbon-carbon bonds by activating alkyl or acyl halides. Its strong Lewis acidity makes it effective in promoting electrophilic substitution processes. It is also employed in the production of other brominated compounds and in certain polymerization reactions. Due to its reactivity with moisture, it is typically handled under anhydrous conditions in industrial and laboratory settings.

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