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Structure of 939-90-2
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rel-(1R,2R)-2-Phenylcyclopropanecarboxylic acid features a rigid cyclopropane scaffold with defined stereochemistry, enabling precise spatial control in asymmetric synthesis. This bench-stable carboxylic acid integrates readily into chiral building blocks for medicinal chemistry and catalytic transformations.
rel-((1R,2R)-2-Phenylcyclopropanecarboxylic acid) serves as a stereochemically defined building block for the synthesis of cyclopropane-containing bioactive molecules. Its rigid chiral framework facilitates controlled functionalization and enables access to pharmaceutically relevant scaffolds through established coupling and derivatization protocols. The compound exhibits bench stability and compatibility with standard synthetic operations, supporting efficient incorporation into complex molecular architectures.
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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: