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Structure of 1344115-77-0
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This boronate ester features a cyclopropylmethyl substituent that enhances stability and modulates reactivity in cross-coupling processes. The tetramethyl-substituted dioxaborolane ring provides excellent bench stability and moisture tolerance, enabling reliable performance under standard conditions. Ideal for Suzuki-Miyaura coupling applications requiring robust, user-friendly reagents.
2-(Cyclopropylmethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate reagent that facilitates Suzuki-Miyaura cross-coupling reactions under mild conditions. Its cyclopropylmethyl group imparts enhanced steric and electronic properties, improving compatibility with diverse electrophiles while maintaining high 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 : H227-H315-H319-H335
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Precautionary Statements : P210-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P403-P405-P501
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Lot numbers can be found on the outside label of a product: