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Structure of 2305-26-2
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This chiral cyclohexene dicarboxylic acid features a rigid, strained ring system with defined stereochemistry at the 1 and 2 positions. The conjugated diene moiety enables participation in Diels-Alder reactions, while the carboxylic acid groups serve as anchor points for derivatization. Bench-stable and moisture-tolerant, it facilitates access to complex cyclic architectures in synthetic organic chemistry and materials design.
(1R,2S)-rel-Cyclohex-4-ene-1,2-dicarboxylic acid serves as a versatile chiral building block in asymmetric synthesis, enabling stereoselective transformations via its rigid bicyclic framework. Its conjugated diene system facilitates Diels–Alder reactions, while the carboxylic acid functionalities offer direct handles for derivatization or salt formation. Bench-stable and readily purified by recrystallization, it functions effectively in natural product synthesis, catalyst design, and pharmaceutical intermediate development.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: