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Structure of 53913-96-5
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tert-Butyl 2-(bromomethyl)prop-2-enoate, 98% (stabilized with MEHQ) features a reactive bromomethyl group conjugated to an enoate moiety, enabling efficient coupling in synthetic transformations. The tert-butyl ester provides stability and ease of handling, while MEHQ prevents radical-induced decomposition. This bench-stable reagent integrates readily into diverse reaction sequences requiring electrophilic alkylating agents.
tert-Butyl 2-(bromomethyl)prop-2-enoate serves as a versatile vinyl-bearing bromide synthon, enabling efficient Michael additions and palladium-catalyzed cross-couplings. The stabilized formulation ensures bench longevity and minimizes decomposition during storage. Its terminal alkene functionality facilitates further derivatization in heterocycle synthesis and late-stage functionalization workflows.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3265
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H302-H314
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Precautionary Statements : P264-P270-P271-P280-P304+P340-P330-P331-P363-P501
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Lot numbers can be found on the outside label of a product: