2-(3,5-Dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

≥98%

Reagent Code: #89942
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CAS Number 365564-07-4

science Other reagents with same CAS 365564-07-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.13 g/mol
Formula C₁₄H₂₁BO₄
thermostat Physical Properties
Melting Point 90-94°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a boronic ester, facilitating the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. This process is crucial in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a valuable reagent for constructing biaryl structures, which are common in many biologically active compounds and functional materials. Additionally, it is employed in the development of organic electronic devices, such as OLEDs, due to its role in creating conjugated polymers and small molecules with specific electronic properties.

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Test Parameter Specification
Appearance White to almost white powder to crystal
Purity 98-100
Melting Point (°C) 88.0-92.0
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿550.00
inventory 1g
10-20 days ฿1,840.00
inventory 5g
10-20 days ฿6,440.00
inventory 25g
10-20 days ฿20,180.00

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2-(3,5-Dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a boronic ester, facilitating the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. This process is crucial in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a valuable reagent for constructing biaryl structures, which are common in many b
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a boronic ester, facilitating the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. This process is crucial in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a valuable reagent for constructing biaryl structures, which are common in many biologically active compounds and functional materials. Additionally, it is employed in the development of organic electronic devices, such as OLEDs, due to its role in creating conjugated polymers and small molecules with specific electronic properties.
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