2-Isopropoxy-4,4,6-trimethyl-1,3,2-dioxaborinane

≥97%(T)

Reagent Code: #199994
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CAS Number 61676-61-7

science Other reagents with same CAS 61676-61-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.06 g/mol
Formula C₉H₁₉BO₃
badge Registry Numbers
MDL Number MFCD15143641
thermostat Physical Properties
Boiling Point 59°C|1.5mmHg(lit.)
inventory_2 Storage & Handling
Density 0.92
Storage Room temperature, dry

description Product Description

Used as a boron-based reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a stable and selective source of boronic acid equivalents, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical manufacturing. Its cyclic structure enhances shelf life and reduces volatility, making it suitable for use in air- and moisture-sensitive reactions. Commonly employed in late-stage functionalization of complex molecules due to its mild reactivity and compatibility with various functional groups.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿480.00
inventory 250mg
10-20 days ฿760.00

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2-Isopropoxy-4,4,6-trimethyl-1,3,2-dioxaborinane
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Used as a boron-based reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a stable and selective source of boronic acid equivalents, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical manufacturing. Its cyclic structure enhances shelf life and reduces volatility, making it suitable for use in air- and moisture-sensitive reactions. Commonly employed in late-stage functionalization of complex molecules due to its

Used as a boron-based reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a stable and selective source of boronic acid equivalents, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical manufacturing. Its cyclic structure enhances shelf life and reduces volatility, making it suitable for use in air- and moisture-sensitive reactions. Commonly employed in late-stage functionalization of complex molecules due to its mild reactivity and compatibility with various functional groups.

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