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Structure of 55685-58-0
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cis-3-Oxabicyclo[3.1.0]hexane-6-carboxylic acid features a rigid, strained bicyclic scaffold with a strategically positioned carboxylic acid group. The fused oxygen atom imparts polarity and enhances solubility, while the cis-configured ring system ensures defined stereochemical control. This structural motif enables precise molecular presentation in synthetic applications requiring constrained geometry and tailored reactivity.
cis-3-Oxabicyclo[3.1.0]hexane-6-carboxylic acid serves as a rigid, bicyclic scaffold for medicinal chemistry and synthetic organic applications. Its constrained geometry enables precise spatial orientation of functional groups, facilitating stereocontrolled synthesis. The carboxylic acid moiety offers direct handle for derivatization, while the oxabridge enhances metabolic stability and modulates physicochemical properties. Bench-stable and compatible with standard coupling protocols, it functions effectively in peptide conjugation and heterocycle construction workflows.
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Lot numbers can be found on the outside label of a product: