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Structure of 4958-02-5
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This cyclobutanecarboxylic acid derivative features a benzyloxy substituent at the 3-position, delivering enhanced solubility and stability in organic media. The aromatic ether moiety facilitates integration into bioactive scaffolds, while the carboxylic acid group enables direct coupling or derivatization under standard conditions.
3-(Benzyloxy)cyclobutanecarboxylic acid serves as a versatile building block for medicinal chemistry and natural product synthesis, enabling the introduction of a rigid cyclobutane scaffold with orthogonal benzyloxy and carboxylic acid functionalities. The molecule exhibits excellent bench stability, facilitates straightforward derivatization via esterification or amide coupling, and supports diverse downstream transformations including hydrogenolysis to release the free alcohol. Its defined stereochemistry and compatibility with standard purification methods make it a practical choice for high-throughput screening campaigns and process-scale applications.
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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: