(E)-2-(4-isopropylstyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

99%

Reagent Code: #183980
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CAS Number 1358754-26-3

science Other reagents with same CAS 1358754-26-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.195 g/mol
Formula C₁₇H₂₅BO₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its vinylboronate ester group participates in palladium-catalyzed couplings with aryl or alkenyl halides, making it valuable in pharmaceutical, agrochemical, and materials chemistry. The isopropyl-substituted styryl group enhances lipophilicity and steric profile, useful in tuning molecular properties during drug discovery. Stable and compatible with various functional groups, it supports modular and efficient synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,320.00
inventory 500mg
10-20 days ฿9,930.00
inventory 1g
10-20 days ฿14,580.00
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(E)-2-(4-isopropylstyryl)-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 the synthesis of complex organic molecules. Its vinylboronate ester group participates in palladium-catalyzed couplings with aryl or alkenyl halides, making it valuable in pharmaceutical, agrochemical, and materials chemistry. The isopropyl-substituted styryl group enhances lipophilicity and steric profile, useful in tuning molecular properties during drug discovery. Stable and compatib

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its vinylboronate ester group participates in palladium-catalyzed couplings with aryl or alkenyl halides, making it valuable in pharmaceutical, agrochemical, and materials chemistry. The isopropyl-substituted styryl group enhances lipophilicity and steric profile, useful in tuning molecular properties during drug discovery. Stable and compatible with various functional groups, it supports modular and efficient synthetic routes.

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