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Structure of 4342-60-3
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4-Methylcyclohex-3-enecarboxylic acid features a conjugated enone system fused with a substituted cyclohexane ring, enabling participation in Diels-Alder reactions and serving as a scaffold for bioactive molecule synthesis. The carboxylic acid group provides a handle for derivatization, while the methyl substituent introduces steric bias that influences regioselectivity. This compound exhibits bench-stable behavior under standard conditions and is compatible with common organic functionalization protocols.
4-Methylcyclohex-3-enecarboxylic acid serves as a versatile building block for functionalized cyclohexene scaffolds, enabling efficient access to bioactive heterocycles and natural product analogs. Its conjugated enone system facilitates Michael additions and Diels–Alder reactions, while the carboxylic acid group supports direct derivatization or coupling protocols. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step synthesis workflows requiring moderate functional group tolerance.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: