Methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline-8-carboxylate

97%

Reagent Code: #207422
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CAS Number 1627722-90-0

science Other reagents with same CAS 1627722-90-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 313.16 g/mol
Formula C₁₇H₂₀BNO₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl halides under palladium catalysis, making it valuable in the preparation of complex quinoline derivatives for drug discovery and materials science. The methyl ester functionality allows further derivatization, enhancing its utility in building bioactive molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿1,170.00
100mg
10-20 days ฿2,830.00
250mg
10-20 days ฿7,070.00
1g
10-20 days ฿28,260.00
5g
10-20 days ฿91,000.00
Methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline-8-carboxylate
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl halides under palladium catalysis, making it valuable in the preparation of complex quinoline derivatives for drug discovery and materials science. The methyl ester functionality allows further derivatization, enhancing its utility in building bioactive molecules.

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl halides under palladium catalysis, making it valuable in the preparation of complex quinoline derivatives for drug discovery and materials science. The methyl ester functionality allows further derivatization, enhancing its utility in building bioactive molecules.

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