2-(3,5-Di-tert-butyl-4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #167215
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CAS Number 1032358-19-2

science Other reagents with same CAS 1032358-19-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 346.31 g/mol
Formula C₂₁H₃₅BO₃
badge Registry Numbers
MDL Number MFCD22493891
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its primary role is as a boronic ester derivative, offering enhanced stability and reactivity under palladium-catalyzed conditions. Commonly employed in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and functional materials. The tert-butyl and methoxy substituents provide steric bulk and electronic effects that improve selectivity and yield in coupling reactions. Suitable for late-stage functionalization due to its tolerance of various functional groups.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿36,300.00
inventory 100mg
10-20 days ฿7,950.00

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2-(3,5-Di-tert-butyl-4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its primary role is as a boronic ester derivative, offering enhanced stability and reactivity under palladium-catalyzed conditions. Commonly employed in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and functional materials. The tert-butyl and methoxy substituents provide steric bulk and electronic effects that improve

Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its primary role is as a boronic ester derivative, offering enhanced stability and reactivity under palladium-catalyzed conditions. Commonly employed in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and functional materials. The tert-butyl and methoxy substituents provide steric bulk and electronic effects that improve selectivity and yield in coupling reactions. Suitable for late-stage functionalization due to its tolerance of various functional groups.

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