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Structure of 696-75-3
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rel-(1R,2R)-Cyclopropane-1,2-dicarboxylic acid features a rigid, chiral cyclopropane core that imparts high stereoselectivity in asymmetric synthesis. The geminal dicarboxylic acid functionality enables direct incorporation into catalytic systems and serves as a robust scaffold for molecular diversity. This bench-stable derivative supports efficient access to bioactive architectures under standard conditions.
rel-(1R,2R)-Cyclopropane-1,2-dicarboxylic acid serves as a versatile chiral building block in synthetic organic chemistry, enabling stereoselective construction of cyclopropane-containing scaffolds. Its rigid, strained ring structure facilitates controlled functionalization and is compatible with standard coupling and derivatization protocols. The compound exhibits bench stability, ease of purification, and tolerance to diverse reaction conditions, making it valuable for medicinal chemistry and materials synthesis workflows.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-H335
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: