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*For research and further manufacturing use only, not for direct human use.
Structure of 2621932-48-5
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This boronate ester features a naphthalene core functionalized with an ethyl, fluoro, and methoxymethoxy group at the 8-, 7-, and 3-positions, respectively. The tetramethyl-substituted dioxaborolane moiety enables stable coupling in Suzuki-Miyaura reactions under standard conditions. Designed for efficient C–C bond formation in complex molecule synthesis, this reagent offers excellent shelf stability and handles well in air-sensitive protocols.
This boronate ester serves as a versatile building block for Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The naphthalene core features orthogonal functional groups—ethyl, fluoro, and methoxymethoxy—that support further derivatization while maintaining stability during storage and handling. Its tetramethyl-substituted dioxaborolane ring enhances shelf life and facilitates purification, making it ideal for iterative synthesis of complex heterocyclic scaffolds and pharmaceutical intermediates.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: