(E)-Non-1-en-1-ylboronic acid

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Reagent Code: #185707
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CAS Number 57404-77-0

science Other reagents with same CAS 57404-77-0

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Weight 170.06 g/mol
Formula C₉H₁₉BO₂
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MDL Number MFCD01074618
inventory_2 Storage & Handling
Storage -20°C, Sealed, Drying, Inert Gas

description Product Description

Used in organic synthesis as a key reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the preparation of complex organic molecules. Its vinylboronic acid structure with an E-configuration double bond allows for stereoselective synthesis, making it valuable in pharmaceutical and agrochemical research. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required. Stable under standard handling conditions, it facilitates efficient coupling with aryl or vinyl halides in the presence of palladium catalysts.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,140.00
inventory 5g
10-20 days ฿60,470.00
inventory 1g
10-20 days ฿14,400.00

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(E)-Non-1-en-1-ylboronic acid
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Used in organic synthesis as a key reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the preparation of complex organic molecules. Its vinylboronic acid structure with an E-configuration double bond allows for stereoselective synthesis, making it valuable in pharmaceutical and agrochemical research. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required. Stable under standard ha
Used in organic synthesis as a key reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the preparation of complex organic molecules. Its vinylboronic acid structure with an E-configuration double bond allows for stereoselective synthesis, making it valuable in pharmaceutical and agrochemical research. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required. Stable under standard handling conditions, it facilitates efficient coupling with aryl or vinyl halides in the presence of palladium catalysts.
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