Tert-butyl 2-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)furan-2-yl)morpholine-4-carboxylate

95%

Reagent Code: #242070
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CAS Number 2223009-14-9

science Other reagents with same CAS 2223009-14-9

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Weight 379.2556 g/mol
Formula C₁₉H₃₀BNO₆
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. The boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable for constructing heterocyclic and functionalized furan derivatives. Its morpholine carboxylate moiety can act as a protecting group or aid in solubility during multi-step syntheses. Commonly employed in drug discovery for building bioactive compound libraries.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿33,840.00
inventory 25mg
10-20 days ฿99,800.00

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Tert-butyl 2-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)furan-2-yl)morpholine-4-carboxylate
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Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. The boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable for constructing heterocyclic and functionalized furan derivatives. Its morpholine carboxylate moiety can act as a protecting group or aid in solubility during multi-step syntheses. Commonly employed in drug discovery for

Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. The boronate ester group facilitates carbon-carbon bond formation under mild conditions, making it valuable for constructing heterocyclic and functionalized furan derivatives. Its morpholine carboxylate moiety can act as a protecting group or aid in solubility during multi-step syntheses. Commonly employed in drug discovery for building bioactive compound libraries.

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