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Structure of 1420859-80-8
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tert-Butyl 3-(2-bromoethyl)azetidine-1-carboxylate delivers a reactive bromoethyl handle on a strained azetidine scaffold, enabling efficient site-specific conjugation. The tert-butyl ester provides stability and convenient deprotection, while the azetidine ring imparts high reactivity for nucleophilic displacement. This combination supports rapid bioconjugation workflows under mild conditions.
tert-Butyl 3-(2-bromoethyl)azetidine-1-carboxylate serves as a versatile building block for the synthesis of azetidine-containing scaffolds, enabling efficient introduction of bromoalkyl functionality. Its stability under standard reaction conditions facilitates downstream functionalization via nucleophilic substitution, palladium-catalyzed coupling, or cyclization reactions. The tert-butyl ester group provides convenient protection and orthogonal handling, simplifying purification and integration into complex molecular architectures relevant to medicinal chemistry and API development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: