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

95%

Reagent Code: #218262
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CAS Number 914606-94-3

science Other reagents with same CAS 914606-94-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 368.2561 g/mol
Formula C₁₆H₂₅BN₂O₅S
badge Registry Numbers
MDL Number MFCD31916433
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl structures. The presence of a morpholine sulfonamide moiety enhances solubility and can influence the electronic properties of the target molecule, aiding in the development of bioactive compounds. It is particularly useful in medicinal chemistry for building drug-like scaffolds with improved metabolic stability and binding affinity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10mg
10-20 days ฿3,590.00
50mg
10-20 days ฿12,230.00
N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]morpholine-4-sulfonamide
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Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl structures. The presence of a morpholine sulfonamide moiety enhances solubility and can influence the electronic properties of the target molecule, ai

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl structures. The presence of a morpholine sulfonamide moiety enhances solubility and can influence the electronic properties of the target molecule, aiding in the development of bioactive compounds. It is particularly useful in medicinal chemistry for building drug-like scaffolds with improved metabolic stability and binding affinity.

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