2-(3,3-Diethoxypropyl)-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane

98%

Reagent Code: #179088
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CAS Number 165904-27-8

science Other reagents with same CAS 165904-27-8

blur_circular Chemical Specifications

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Weight 258.16 g/mol
Formula C₁₃H₂₇BO₄
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MDL Number MFCD03788723
inventory_2 Storage & Handling
Storage Room temperature

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Used as a key reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds. Its boron-containing structure allows for efficient transformation into various functional groups, making it valuable in pharmaceutical and agrochemical synthesis. The diethoxypropyl group enhances stability and solubility, improving handling and reactivity in multi-step synthetic routes. Commonly employed in the preparation of complex organic molecules, including bioactive compounds and functional materials.

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inventory 100mg
10-20 days ฿5,480.00

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2-(3,3-Diethoxypropyl)-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane
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Used as a key reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds. Its boron-containing structure allows for efficient transformation into various functional groups, making it valuable in pharmaceutical and agrochemical synthesis. The diethoxypropyl group enhances stability and solubility, improving handling and reactivity in multi-step synthetic routes. Commonly employed in the preparation of complex organi

Used as a key reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds. Its boron-containing structure allows for efficient transformation into various functional groups, making it valuable in pharmaceutical and agrochemical synthesis. The diethoxypropyl group enhances stability and solubility, improving handling and reactivity in multi-step synthetic routes. Commonly employed in the preparation of complex organic molecules, including bioactive compounds and functional materials.

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