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Structure of 74080-50-5
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This chiral alcohol features a conjugated enol system and a stereodefined methyl group at C3, enabling selective transformations in asymmetric synthesis. The (2R,3R) configuration ensures predictable stereochemical outcomes in cascade reactions and coupling processes under standard conditions.
(2R,3R)-3-Methylpent-4-en-2-ol serves as a stereochemically defined building block for the synthesis of chiral intermediates in natural product and pharmaceutical research. Its conjugated enol functionality enables reliable transformations in aldol-type reactions and metal-catalyzed additions, while the stable stereocenters facilitate predictable stereochemical outcomes. The molecule exhibits good bench stability and is readily purified by distillation or chromatography, making it well-suited for iterative synthetic sequences requiring high diastereoselectivity.
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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#: 1987
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H225-H315-H319-H335
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: