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Structure of 3289-19-8
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This boronate moiety integrates a chiral, bench-stable 1,3-dioxolane scaffold with a primary amine functionality. The methanamine group enables direct conjugation or derivatization in synthetic workflows. Designed for stability under standard conditions, it facilitates efficient access to functionalized intermediates in medicinal chemistry and materials synthesis.
(2-Methyl-1,3-dioxolan-2-yl)methanamine serves as a stable, bench-friendly synthon for introducing the 2-methyl-1,3-dioxolane-2-ylmethyl group in synthetic sequences. It functions as a protected hydroxymethyl equivalent and enables selective nucleophilic transformations under mild conditions. The molecule exhibits excellent functional group tolerance and facilitates efficient coupling reactions, making it particularly useful in the construction of heterocyclic scaffolds and complex molecular architectures relevant to medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 1993
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H225-H315-H319
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P264-P280-P362+P364-P370+P378-P501
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Lot numbers can be found on the outside label of a product: