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Structure of 88335-93-7
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This cyclohexene derivative features a strategically positioned methoxycarbonyl group and carboxylic acid functionality, enabling direct integration into synthetic routes requiring both ester and acid handles. The rigid, unsaturated backbone provides defined stereochemistry for asymmetric synthesis applications.
(1R,6S)-6-(Methoxycarbonyl)cyclohex-3-ene-1-carboxylic acid serves as a versatile chiral building block for the synthesis of substituted cyclohexane derivatives and heterocyclic scaffolds. Its conjugated diene system enables Diels-Alder reactions with high stereoselectivity, while the orthogonal functionality of the ester and carboxylic acid groups supports sequential transformations. Bench-stable and amenable to purification by standard chromatography, it facilitates efficient access to complex molecular 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 : H315-H319-H335
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Precautionary Statements : P302+P352-P304+P340-P362-P501
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Lot numbers can be found on the outside label of a product: