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Structure of 1338377-73-3
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(1S)-1-Cyclopropyl-2,2,2-trifluoroethan-1-amine hydrochloride delivers a chiral trifluoromethylated amine scaffold with enhanced metabolic stability. The cyclopropyl group imparts conformational rigidity, while the trifluoroethanol moiety provides strong electron-withdrawing character. This bench-stable salt facilitates direct incorporation into bioactive molecules and supports efficient synthetic access to fluorinated pharmaceutical intermediates under standard conditions.
(1S)-1-Cyclopropyl-2,2,2-trifluoroethan-1-amine hydrochloride serves as a stereochemically defined building block for fluorinated bioactive molecules. Its trifluoromethyl group enhances metabolic stability and membrane permeability, while the cyclopropyl moiety imparts conformational rigidity. The amine functionality enables straightforward derivatization via amidation, alkylation, or reductive amination, facilitating rapid access to diverse scaffolds in medicinal chemistry campaigns. Bench-stable and readily purified by standard methods, it supports scalable synthesis of target compounds with predictable stereochemical fidelity.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: