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Structure of 23020-15-7
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This chiral cyclopropane carboxylic acid features a rigid, strained three-membered ring fused to a phenyl group, enabling precise stereochemical control in asymmetric synthesis. The carboxylate moiety offers versatile derivatization potential while maintaining structural integrity under standard conditions.
(1S,2S)-2-Phenylcyclopropane-1-carboxylic acid serves as a rigid, chiral building block for medicinal chemistry and asymmetric synthesis. Its cyclopropanecarboxylic acid scaffold enables stereoselective transformations and functions as a structural motif in bioactive molecule design. The compound exhibits bench stability, facilitates efficient derivatization via standard carboxylic acid reactions, and supports orthogonal functional group manipulation in complex synthetic sequences.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: