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Structure of 62563-07-9
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This dioxolane derivative features a bromopropyl chain enabling direct functionalization in synthetic sequences. The cyclic acetal scaffold enhances stability and solubility, while the terminal bromide supports efficient coupling reactions under mild conditions. A reliable handle for building complex architectures in organic synthesis and medicinal chemistry workflows.
2-(3-Bromopropyl)-1,3-dioxolane serves as a versatile bifunctional building block for the synthesis of complex heterocycles and bioactive molecules. The bromide functionality enables efficient alkylation or transition-metal-catalyzed coupling reactions, while the 1,3-dioxolane ring provides stability and orthogonality under basic conditions. This compound facilitates the construction of pharmacophoric scaffolds with predictable reactivity, offering reliable access to intermediates in medicinal chemistry campaigns.
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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#: 1993
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H227
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Precautionary Statements : P210-P280-P501
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Lot numbers can be found on the outside label of a product: