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Structure of 67562-19-0
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4,4,5,5-Tetramethyl-2-propyl-1,3,2-dioxaborolane is a bench-stable boronate reagent featuring a sterically protected boronate moiety and a propyl substituent that enhances solubility in organic solvents. This structure enables efficient coupling in Suzuki-Miyaura reactions under mild conditions, offering reliable performance in complex molecule synthesis.
4,4,5,5-Tetramethyl-2-propyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. Its sterically hindered dioxaborolane core enhances hydrolytic stability and functional group tolerance, enabling reliable coupling with aryl, vinyl, and heteroaryl halides under standard conditions. The propyl substituent improves solubility in organic media, facilitating purification and scalability in complex molecule synthesis.
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GHS Pictogram :
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GHS No : GHS02
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Signal Word : Danger
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UN#: 3272
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H225
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P280-P370+P378-P501
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Lot numbers can be found on the outside label of a product: