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Structure of 14590-52-4
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This chiral cyclopropanecarboxylic acid features a rigid, strained ring system that imparts distinctive conformational control. The (1S,2S) stereochemistry enables precise spatial orientation in synthetic applications, while the methyl substituent enhances steric definition. This bench-stable derivative integrates readily into complex molecular architectures requiring defined geometry and stability under standard conditions.
(1S,2S)-2-Methylcyclopropanecarboxylic acid serves as a stereochemically defined building block for the synthesis of bioactive cyclopropyl-containing compounds. Its rigid cyclopropane scaffold imparts conformational restraint, enabling precise spatial orientation in medicinal chemistry applications. The carboxylic acid functionality facilitates direct derivatization or coupling reactions, while the chiral centers ensure enantioselective access to target molecules. Bench-stable and compatible with standard synthetic protocols, it functions effectively in peptide mimetics, agrochemical intermediates, and heterocyclic ring systems.
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3265
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Class : 8
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Packing Group : Ⅲ
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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: