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Structure of 138326-68-8
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(S)-Methyl 2-amino-2-cyclopropylacetate hydrochloride features a chiral cyclopropyl scaffold that imparts distinct stereochemical control in asymmetric synthesis. The amine functionality enables direct derivatization, while the hydrochloride salt enhances solubility and stability under standard handling conditions. This compound serves as a key building block for bioactive molecules requiring defined stereocenters.
(S)-Methyl 2-amino-2-cyclopropylacetate hydrochloride serves as a stereochemically defined building block for the synthesis of bioactive molecules, particularly in medicinal chemistry. Its cyclopropyl moiety imparts conformational rigidity, while the protected amine and ester functionalities enable orthogonal transformations. The compound exhibits excellent bench stability and facilitates efficient coupling reactions, making it well-suited for modular peptide and heterocycle construction.
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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: