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Structure of 1375302-99-0
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This boronate ester features a pyridine core functionalized with a benzyloxy group at the 3-position and a tetramethyl-dioxaborolane moiety at the 5-position. The pendant benzyl ether enhances solubility and stability, while the diborane handle enables efficient Suzuki-Miyaura coupling under standard conditions. Designed for streamlined C–C bond formation in complex molecular architectures.
3-(Benzyloxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The pyridine core enables efficient functionalization in medicinal chemistry and materials synthesis, while the benzyloxy group provides orthogonal protection and enhanced solubility. The stable tetramethylboronate moiety facilitates reliable coupling under mild conditions, with excellent functional group tolerance and ease of purification.
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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: