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Structure of 122763-67-1
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tert-Butyl 3-hydroxypent-4-enoate, stabilized with MEHQ, features a conjugated enol ether system and a pendant hydroxyl group, enabling direct incorporation into complex synthetic sequences. The tert-butyl ester enhances stability under standard conditions while the MEHQ additive suppresses radical-mediated degradation. This bench-stable reagent facilitates efficient access to functionalized carbocycles and heterocycles via tandem cyclization or cycloaddition processes.
tert-Butyl 3-hydroxypent-4-enoate, stabilized with MEHQ, serves as a versatile β-hydroxy enoate building block for synthetic applications. Its conjugated enone system enables reliable Michael additions and aldol-type cyclizations, while the tert-butyl ester provides excellent bench stability and ease of purification. The hydroxyl group offers direct handle for functionalization, and the stabilizing agent prevents premature polymerization, ensuring consistent performance in multi-step syntheses.
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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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: