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Structure of 5708-19-0
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(S)-cyclohex-3-enecarboxylic acid is a chiral, bench-stable building block featuring a conjugated enoic acid moiety within a rigid cyclohexene framework. This configuration enables stereoselective transformations in asymmetric synthesis, particularly in the construction of functionalized cyclic systems via Michael additions or Diels–Alder reactions.
(S)-cyclohex-3-enecarboxylic acid serves as a valuable chiral building block for the synthesis of bioactive molecules and natural product analogs. Its conjugated alkene and carboxylic acid functionality enables direct use in coupling reactions, hydrogenation, and functionalization workflows. The stereochemistry at the cyclohexene ring facilitates controlled stereoselective transformations, offering predictable regiochemical outcomes in asymmetric synthesis. Bench-stable and readily purified, it functions effectively in both academic and industrial R&D settings.
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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 : Ⅲ
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Hazard Statements : H312-H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: