4,4,5,5-Tetramethyl-2-(o-tolyl)-1,3,2-dioxaborolane

>97.0%(GC)(T)

Reagent Code: #90304
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CAS Number 195062-59-0

science Other reagents with same CAS 195062-59-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.1 g/mol
Formula C₁₃H₁₉BO₂
badge Registry Numbers
MDL Number MFCD06795658
thermostat Physical Properties
Melting Point 18°C (凝固点)
inventory_2 Storage & Handling
Density 0.99g/mL
Storage Room temperature, dry, inert gas storage

description Product Description

This chemical is primarily used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boron source, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a valuable tool in the preparation of biaryl compounds, which are essential in drug discovery and material science. Additionally, it is employed in the development of polymers and electronic materials due to its ability to introduce boron-containing functional groups into organic frameworks.

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Test Parameter Specification
Appearance Colorless Liquid
Purity (%) 97-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿450.00
inventory 5g
10-20 days ฿2,070.00

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4,4,5,5-Tetramethyl-2-(o-tolyl)-1,3,2-dioxaborolane
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This chemical is primarily used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boron source, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a valuable tool in the preparation of biaryl compounds, which are essential in drug discovery and material science. Additionally, it is employed in the developmen

This chemical is primarily used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boron source, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a valuable tool in the preparation of biaryl compounds, which are essential in drug discovery and material science. Additionally, it is employed in the development of polymers and electronic materials due to its ability to introduce boron-containing functional groups into organic frameworks.

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