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*For research and further manufacturing use only, not for direct human use.
Structure of 380499-68-3
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This boronate-functional acyl chloride integrates seamlessly into Suzuki-Miyaura coupling workflows, offering rapid access to biaryl ketones under mild conditions. The tetramethyl-1,3,2-dioxaborolane moiety ensures high stability and moisture tolerance, while the reactive acyl chloride group enables direct conjugation with nucleophiles.
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoyl chloride serves as a versatile building block for Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and aryl ketone scaffolds. The boronate ester moiety provides excellent stability and functional group tolerance, while the acyl chloride reacts readily with amines and alcohols, facilitating downstream derivatization. Its bench-stable nature and compatibility with standard coupling conditions make it ideal for medicinal chemistry and process development workflows.
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 2923
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Class : 8 (6.1)
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H314-H331
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: