2-(pyrrolidin-1-yl)-N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethane-1-sulfonamide

95%

Reagent Code: #218331
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CAS Number 756520-86-2

science Other reagents with same CAS 756520-86-2

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Weight 380.30986 g/mol
Formula C₁₈H₂₉BN₂O₄S
badge Registry Numbers
MDL Number MFCD32206543
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of sulfonamide-based bioactive molecules, including kinase inhibitors and receptor antagonists. Valued for high stability and reactivity in palladium-catalyzed transformations.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿23,680.00
inventory 1g
10-20 days ฿56,000.00

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2-(pyrrolidin-1-yl)-N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethane-1-sulfonamide
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of sulfonamide-based bioactive molecules, including kinase inhibitors and receptor antagonists. Valued for high stability and reactivity in palladium-catalyzed transformations.

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of sulfonamide-based bioactive molecules, including kinase inhibitors and receptor antagonists. Valued for high stability and reactivity in palladium-catalyzed transformations.

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