2-Morpholino-5-trifluoromethylphenylboronic acid pinacol ester

95%

Reagent Code: #214241
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CAS Number 906352-77-0

science Other reagents with same CAS 906352-77-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 357.18 g/mol
Formula C₁₇H₂₃BF₃NO₃
badge Registry Numbers
MDL Number MFCD09064984
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester group facilitates efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for constructing biaryl scaffolds. The presence of the morpholino and trifluoromethyl groups enhances electronic and metabolic stability, which is beneficial in designing bioactive compounds. Commonly employed in medicinal chemistry for lead optimization and library synthesis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿40,290.00
2-Morpholino-5-trifluoromethylphenylboronic acid pinacol ester
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester group facilitates efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for constructing biaryl scaffolds. The presence of the morpholino and trifluoromethyl groups enhances electronic and metabolic stability, which is beneficial in designing bioactive compounds.

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester group facilitates efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for constructing biaryl scaffolds. The presence of the morpholino and trifluoromethyl groups enhances electronic and metabolic stability, which is beneficial in designing bioactive compounds. Commonly employed in medicinal chemistry for lead optimization and library synthesis.

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