N-(2,4-Difluorophenyl)-2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-sulfonamide

95%

Reagent Code: #218761
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CAS Number 1383992-65-1

science Other reagents with same CAS 1383992-65-1

blur_circular Chemical Specifications

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Weight 426.3 g/mol
Formula C₁₈H₂₁BF₂N₂O₅S
inventory_2 Storage & Handling
Storage 2-8°C, dry, closed

description Product Description

Used as an 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 applied in the development of sulfonamide-based bioactive molecules, including kinase inhibitors and antifungal agents. Valued for its stability and reactivity in palladium-catalyzed transformations during drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿76,080.00
N-(2,4-Difluorophenyl)-2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-sulfonamide
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Used as an 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 applied in the development of sulfonamide-based bioactive molecules, including kinase inhibitors and antifungal agents. Valued for its stability and reactivity in palladium-catalyzed transformations during drug discovery.

Used as an 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 applied in the development of sulfonamide-based bioactive molecules, including kinase inhibitors and antifungal agents. Valued for its stability and reactivity in palladium-catalyzed transformations during drug discovery.

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