1,3,2-Dioxaborolane, 2-[4-[(2-chlorophenyl)methoxy]phenyl]-4,4,5,5-tetramethyl-

95%

Reagent Code: #176238
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CAS Number 854371-84-9

science Other reagents with same CAS 854371-84-9

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Weight 344.64 g/mol
Formula C₁₉H₂₂BClO₃
badge Registry Numbers
MDL Number MFCD22494050
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boron-containing structure allows it to react with aryl halides in the presence of palladium catalysts, enabling the construction of complex aromatic systems found in pharmaceuticals and agrochemicals. The chlorophenyl and phenyl ether groups provide specific electronic and steric properties that influence reactivity and selectivity in coupling processes. Commonly employed in the development of active pharmaceutical ingredients where tailored aromatic frameworks are required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,680.00
inventory 250mg
10-20 days ฿11,680.00
inventory 1g
10-20 days ฿19,320.00

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1,3,2-Dioxaborolane, 2-[4-[(2-chlorophenyl)methoxy]phenyl]-4,4,5,5-tetramethyl-
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Used as an intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boron-containing structure allows it to react with aryl halides in the presence of palladium catalysts, enabling the construction of complex aromatic systems found in pharmaceuticals and agrochemicals. The chlorophenyl and phenyl ether groups provide specific electronic and steric properties that influence reactivity and selectivity in coupling processes. Commonly employed in t
Used as an intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boron-containing structure allows it to react with aryl halides in the presence of palladium catalysts, enabling the construction of complex aromatic systems found in pharmaceuticals and agrochemicals. The chlorophenyl and phenyl ether groups provide specific electronic and steric properties that influence reactivity and selectivity in coupling processes. Commonly employed in the development of active pharmaceutical ingredients where tailored aromatic frameworks are required.
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