2-[(3,5-Difluorophenyl)methyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #42203
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CAS Number 1392150-21-8

science Other reagents with same CAS 1392150-21-8

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Weight 254.08 g/mol
Formula C₁₃H₁₇BF₂O₂
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MDL Number MFCD31457494
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description Product Description

This chemical is primarily utilized in organic synthesis as a boron-containing reagent, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for introducing the 3,5-difluorobenzyl group into more complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. Its stability and reactivity make it suitable for constructing carbon-carbon bonds in the synthesis of bioactive compounds, including potential drug candidates. Additionally, it is employed in materials science for the preparation of boron-based polymers and advanced materials with specific electronic or optical properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿18,162.00
inventory 1g
10-20 days ฿48,438.00
inventory 100mg
10-20 days ฿10,890.00

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2-[(3,5-Difluorophenyl)methyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This chemical is primarily utilized in organic synthesis as a boron-containing reagent, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for introducing the 3,5-difluorobenzyl group into more complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. Its stability and reactivity make it suitable for constructing carbon-carbon bonds in the synthesis of bioactive compounds, including potential drug candidates. Additionally, it is em

This chemical is primarily utilized in organic synthesis as a boron-containing reagent, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for introducing the 3,5-difluorobenzyl group into more complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. Its stability and reactivity make it suitable for constructing carbon-carbon bonds in the synthesis of bioactive compounds, including potential drug candidates. Additionally, it is employed in materials science for the preparation of boron-based polymers and advanced materials with specific electronic or optical properties.

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