(Z)-2-(But-2-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #91225
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CAS Number 69611-01-4

science Other reagents with same CAS 69611-01-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.0677 g/mol
Formula C₁₀H₁₉BO₂
badge Registry Numbers
MDL Number MFCD09842772
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This (Z)-configured alkenylboronic acid pinacol ester is primarily utilized in organic synthesis as a reagent for cross-coupling reactions, notably the Suzuki-Miyaura reaction. It facilitates the stereospecific transfer of the (Z)-but-2-en-1-yl group to form carbon-carbon bonds with aryl or vinyl halides, enabling the efficient assembly of complex organic molecules in pharmaceutical, agrochemical, and fine chemical applications. The compound's stability under diverse reaction conditions also supports its use in materials science for incorporating alkenyl functionalities into polymers and other advanced structures.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,704.00
inventory 1g
10-20 days ฿20,295.00
inventory 5g
10-20 days ฿55,440.00

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(Z)-2-(But-2-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This (Z)-configured alkenylboronic acid pinacol ester is primarily utilized in organic synthesis as a reagent for cross-coupling reactions, notably the Suzuki-Miyaura reaction. It facilitates the stereospecific transfer of the (Z)-but-2-en-1-yl group to form carbon-carbon bonds with aryl or vinyl halides, enabling the efficient assembly of complex organic molecules in pharmaceutical, agrochemical, and fine chemical applications. The compound's stability under diverse reaction conditions also supports its

This (Z)-configured alkenylboronic acid pinacol ester is primarily utilized in organic synthesis as a reagent for cross-coupling reactions, notably the Suzuki-Miyaura reaction. It facilitates the stereospecific transfer of the (Z)-but-2-en-1-yl group to form carbon-carbon bonds with aryl or vinyl halides, enabling the efficient assembly of complex organic molecules in pharmaceutical, agrochemical, and fine chemical applications. The compound's stability under diverse reaction conditions also supports its use in materials science for incorporating alkenyl functionalities into polymers and other advanced structures.

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