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Structure of 34669-51-7
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This chiral cyclopropane carboxylic acid features a rigid three-membered ring with defined stereochemistry at the 1,2,3-positions. The dimethyl substitution enhances structural stability and influences conformational rigidity, making it valuable for asymmetric synthesis and as a scaffold in medicinal chemistry.
(1R,2R,3S)-2,3-Dimethylcyclopropane-1-carboxylic acid serves as a rigid, stereochemically defined building block for medicinal chemistry and natural product synthesis. Its cyclopropane core imparts conformational constraint, enabling precise spatial control in bioactive molecule design. The carboxylic acid functionality facilitates direct derivatization via esterification, amidation, or coupling reactions. Bench-stable and amenable to purification by standard chromatographic methods, it functions reliably in multi-step syntheses requiring stereoselective construction of quaternary centers.
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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 : Ⅱ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: