2-(3,4-Dihydro-2H-pyran-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95% (stabilized with 1%BHT)

Reagent Code: #175830
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CAS Number 1025707-93-0

science Other reagents with same CAS 1025707-93-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.08 g/mol
Formula C₁₁H₁₉BO₃
badge Registry Numbers
MDL Number MFCD07368233
thermostat Physical Properties
Boiling Point 240.9°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, stored in inert gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Its boronate ester group is highly reactive with aryl and vinyl halides in the presence of palladium catalysts, making it valuable in pharmaceutical synthesis and materials science. The dihydropyran ring offers a handle for further functionalization or protection strategies in multistep syntheses. Commonly employed in the preparation of bioactive compounds and conjugated systems for optoelectronic applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿540.00
inventory 250mg
10-20 days ฿1,070.00
inventory 1g
10-20 days ฿2,870.00
inventory 5g
10-20 days ฿10,640.00

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2-(3,4-Dihydro-2H-pyran-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Its boronate ester group is highly reactive with aryl and vinyl halides in the presence of palladium catalysts, making it valuable in pharmaceutical synthesis and materials science. The dihydropyran ring offers a handle for further functionalization or protection strategies in multistep syntheses. Commonly employed in the preparation of bioactive compounds and

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. Its boronate ester group is highly reactive with aryl and vinyl halides in the presence of palladium catalysts, making it valuable in pharmaceutical synthesis and materials science. The dihydropyran ring offers a handle for further functionalization or protection strategies in multistep syntheses. Commonly employed in the preparation of bioactive compounds and conjugated systems for optoelectronic applications.

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