Boron tribromide

99.999% metals basis

Reagent Code: #143042
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Alias Boron tribromide; boron bromide, natural alkali
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CAS Number 10294-33-4

science Other reagents with same CAS 10294-33-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.52 g/mol
Formula BBr₃
badge Registry Numbers
EC Number 233-657-9
MDL Number MFCD00011312
thermostat Physical Properties
Melting Point −46 °C(lit.)
Boiling Point ~90 °C
inventory_2 Storage & Handling
Density 2.60 g/mL at 20 °C(lit.)
Storage 2-8℃, avoid light, and fill with argon

description Product Description

Widely used in organic synthesis, particularly for the cleavage of methyl ethers. It efficiently removes methyl groups from aromatic and aliphatic methyl ethers, making it valuable in the preparation of phenols and other oxygen-containing compounds. Commonly employed in pharmaceutical manufacturing where selective deprotection of ether functionalities is required. Also used in the synthesis of advanced intermediates in fine chemicals and agrochemicals. Due to its strong Lewis acidity, it serves as a catalyst in various electrophilic reactions, including bromination and alkylation processes. Additionally, it is used in the semiconductor industry as a boron source for doping processes. Handles under inert conditions because of its high reactivity with moisture and air.

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inventory 25g
10-20 days ฿22,000.00

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Boron tribromide
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Widely used in organic synthesis, particularly for the cleavage of methyl ethers. It efficiently removes methyl groups from aromatic and aliphatic methyl ethers, making it valuable in the preparation of phenols and other oxygen-containing compounds. Commonly employed in pharmaceutical manufacturing where selective deprotection of ether functionalities is required. Also used in the synthesis of advanced intermediates in fine chemicals and agrochemicals. Due to its strong Lewis acidity, it serves as a cata

Widely used in organic synthesis, particularly for the cleavage of methyl ethers. It efficiently removes methyl groups from aromatic and aliphatic methyl ethers, making it valuable in the preparation of phenols and other oxygen-containing compounds. Commonly employed in pharmaceutical manufacturing where selective deprotection of ether functionalities is required. Also used in the synthesis of advanced intermediates in fine chemicals and agrochemicals. Due to its strong Lewis acidity, it serves as a catalyst in various electrophilic reactions, including bromination and alkylation processes. Additionally, it is used in the semiconductor industry as a boron source for doping processes. Handles under inert conditions because of its high reactivity with moisture and air.

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