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Structure of 121250-04-2
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(R)-3,3,3-Trifluoro-2-hydroxypropanoic acid features a chiral center flanked by a trifluoromethyl group and a hydroxyl-bearing carbon, delivering high polarity and enhanced metabolic stability. This configuration enables precise stereochemical control in asymmetric synthesis, particularly as a building block for fluorinated bioactive molecules and enzyme inhibitors.
(R)-3,3,3-Trifluoro-2-hydroxypropanoic acid serves as a valuable chiral building block for fluorinated β-hydroxy carboxylic acid scaffolds. Its well-defined stereochemistry and trifluoromethyl group enable predictable reactivity in esterification, amidation, and coupling reactions. The molecule exhibits bench stability and facilitates access to fluorinated intermediates relevant to medicinal chemistry and agrochemical synthesis.
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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: