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Structure of 31420-47-0
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This cyclopropane derivative features a methoxycarbonyl group at C2 and a carboxylic acid at C1, configured as (1S,2R). The rigid cyclopropane ring imparts distinct stereochemical control, enabling precise incorporation into complex molecular architectures. The ester functionality enhances solubility and facilitates downstream transformations under standard conditions.
rel-((1S,2R)-2-(Methoxycarbonyl)cyclopropane-1-carboxylic acid) serves as a versatile chiral building block in synthetic organic chemistry, enabling the construction of bioactive cyclopropyl motifs found in pharmaceuticals and agrochemicals. Its defined stereochemistry facilitates high diastereoselective transformations, while the ester and carboxylic acid functionalities offer orthogonal handles for downstream derivatization. The compound exhibits good bench stability and is amenable to standard purification methods, making it well-suited for iterative synthesis workflows.
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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: