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Structure of 1196154-75-2
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This trifluorinated amino alcohol hydrochloride delivers a polar, bench-stable scaffold with enhanced solubility and metabolic stability. The electron-withdrawing trifluoromethyl group modulates reactivity, while the protonated amine enables efficient salt formation for purification and formulation. Ideal for medicinal chemistry campaigns requiring bioavailable, fluorinated building blocks.
2-Amino-3,3,3-trifluoropropan-1-ol hydrochloride serves as a versatile building block in medicinal chemistry, enabling the synthesis of fluorinated amino alcohols with enhanced metabolic stability. Its trifluoromethyl group imparts strong electron-withdrawing character and improved lipophilicity, while the primary amine and hydroxyl functionalities offer orthogonal reactivity for conjugation or derivatization. The hydrochloride salt enhances bench stability and solubility, facilitating handling in standard synthetic workflows.
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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: