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Structure of 55780-88-6
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This bicyclic scaffold features a rigid, oxygen-bridged ring system with defined stereochemistry at the 1,5,6 positions. The carboxylic acid group provides a handle for derivatization, while the strained framework imparts unique conformational control. Ideal for probing steric and electronic effects in synthetic applications.
(1R,5S,6R)-rel-3-Oxabicyclo[3.1.0]hexane-6-carboxylic acid serves as a rigid, conformationally constrained scaffold for medicinal and synthetic chemistry applications. Its bicyclic structure imparts defined stereochemistry and spatial rigidity, enabling precise control in ligand design and target engagement studies. The carboxylic acid functionality facilitates derivatization via amide bond formation or esterification, while the ether bridge enhances metabolic stability. This compound functions as a valuable building block in the synthesis of bioactive heterocycles and serves as a key structural motif in lead optimization campaigns requiring defined molecular topology.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: