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*For research and further manufacturing use only, not for direct human use.
Structure of 1279090-25-3
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This boronate-functionalized oxetane integrates seamlessly into late-stage C–H borylation and Suzuki-Miyaura coupling workflows. The tert-butyl carbamate protects the amine while the oxetane ring enhances solubility and metabolic stability, enabling efficient incorporation into complex molecular architectures under standard conditions.
tert-Butyl (3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)oxetan-3-yl)carbamate serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. The oxetane ring imparts enhanced metabolic stability and improved physicochemical properties in medicinal chemistry applications. The boronate group exhibits high functional group tolerance and bench stability, facilitating straightforward purification and integration into complex molecular architectures.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: