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Structure of 30132-23-1
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Ethyl 3-bromo-2-oxocyclohexanecarboxylate features a brominated cyclohexanone scaffold with high reactivity at the C3 position. This electrophilic site enables efficient alkylation and conjugate addition reactions, making it a valuable intermediate in synthetic routes to complex heterocycles and natural product analogs. The ester functionality supports further transformations under standard conditions.
Ethyl 3-bromo-2-oxocyclohexanecarboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of functionalized cyclohexane scaffolds. The α-bromoketone moiety facilitates nucleophilic substitution and enolate-based transformations, while the ester group supports selective reduction or hydrolysis. Its bench-stable nature and compatibility with standard coupling reactions make it ideal for iterative synthesis of complex cyclic architectures in medicinal chemistry and natural product synthesis.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: