Boron Trichloride - 2-Chloroethanol Reagent

(5-10%)[for esterification]

Reagent Code: #77856
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CAS Number 75507-65-2

science Other reagents with same CAS 75507-65-2

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badge Registry Numbers
MDL Number MFCD00060147
inventory_2 Storage & Handling
Storage -20°C, stored with argon

description Product Description

The Boron Trichloride - 2-Chloroethanol Reagent is primarily used in organic synthesis for the cleavage of methyl ethers, particularly in the deprotection of methoxy groups in aromatic compounds. This reagent is highly effective in converting methoxy groups into hydroxyl groups, which is a critical step in the synthesis of various pharmaceuticals and fine chemicals. It is also employed in the preparation of boron-containing compounds, which are useful in materials science and catalysis. Additionally, this reagent finds application in the modification of polymers and resins, enhancing their properties for specific industrial uses. Its ability to selectively react with certain functional groups makes it a valuable tool in complex chemical transformations.

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Test Parameter Specification
Appearance Colorless to almost colorless clear liquid
Concentration (Neutralization Titration) 5.0-10.0% w/w
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1ml
10-20 days ฿1,720.00

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Boron Trichloride - 2-Chloroethanol Reagent
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The Boron Trichloride - 2-Chloroethanol Reagent is primarily used in organic synthesis for the cleavage of methyl ethers, particularly in the deprotection of methoxy groups in aromatic compounds. This reagent is highly effective in converting methoxy groups into hydroxyl groups, which is a critical step in the synthesis of various pharmaceuticals and fine chemicals. It is also employed in the preparation of boron-containing compounds, which are useful in materials science and catalysis. Additionally, thi

The Boron Trichloride - 2-Chloroethanol Reagent is primarily used in organic synthesis for the cleavage of methyl ethers, particularly in the deprotection of methoxy groups in aromatic compounds. This reagent is highly effective in converting methoxy groups into hydroxyl groups, which is a critical step in the synthesis of various pharmaceuticals and fine chemicals. It is also employed in the preparation of boron-containing compounds, which are useful in materials science and catalysis. Additionally, this reagent finds application in the modification of polymers and resins, enhancing their properties for specific industrial uses. Its ability to selectively react with certain functional groups makes it a valuable tool in complex chemical transformations.

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