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Structure of 17202-64-1
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Spiro[2.2]pentane-1-carboxylic acid delivers a rigid, three-dimensional scaffold with enhanced metabolic stability and improved solubility profiles. The spirocyclic core resists conformational flexibility, while the carboxylic acid group enables direct conjugation or derivatization under standard conditions. This structure facilitates efficient incorporation into bioactive molecules requiring steric shielding and controlled polarity.
Spiro[2.2]pentane-1-carboxylic acid serves as a rigid, bicyclic building block for medicinal chemistry and materials science, offering enhanced metabolic stability and conformational constraint. Its carboxylic acid functionality enables direct derivatization via standard coupling reactions, while the spirocyclic core imparts excellent bench stability and orthogonal reactivity in multi-step syntheses.
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Lot numbers can be found on the outside label of a product: