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Structure of 4771-80-6
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Cyclohex-3-enecarboxylic acid features a conjugated enone system that enhances reactivity in Diels-Alder and Michael addition reactions. The carboxylic acid group provides a handle for derivatization, while the rigid cyclohexene backbone offers defined stereochemical control in synthetic transformations.
Cyclohex-3-enecarboxylic acid serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized cyclohexane derivatives. Its conjugated enone-like structure facilitates electrophilic additions, Diels–Alder reactions, and metal-catalyzed transformations. The carboxylic acid group provides a handle for derivatization via esterification, amidation, or decarboxylation protocols. Bench-stable and readily purified by recrystallization, it functions effectively in multi-step syntheses of natural product analogs and pharmaceutical intermediates.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H312-H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P302+P352-P304+P340-P362+P364-P363-P405-P501
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Lot numbers can be found on the outside label of a product: