N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]morpholine-4-sulfonamide
95%
- Product Code: 218262
CAS:
914606-94-3
Molecular Weight: | 368.2561 g./mol | Molecular Formula: | C₁₆H₂₅BN₂O₅S |
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EC Number: | MDL Number: | MFCD31916433 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature |
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.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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10mg | 10-20 days | €94.61 |
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50mg | 10-20 days | €322.30 |
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N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]morpholine-4-sulfonamide
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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