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Structure of 22038-85-3
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(R)-2,2,2-Trifluoro-1-phenylethan-1-amine is a chiral amine featuring a trifluoromethyl group adjacent to a phenyl-substituted carbon. This configuration imparts enhanced lipophilicity and metabolic stability, enabling its use in asymmetric synthesis and as a building block for bioactive molecules. The stereogenic center ensures high enantioselectivity in catalytic transformations.
(R)-2,2,2-Trifluoro-1-phenylethan-1-amine serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of fluorinated phenethylamine derivatives with defined stereochemistry. Its trifluoromethyl group imparts enhanced metabolic stability and lipophilicity, while the primary amine facilitates straightforward functionalization. The compound exhibits good bench stability and is compatible with standard coupling and reduction protocols, making it well-suited for iterative synthetic sequences in API development.
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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#: 3259
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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 : P280-P301+P330+P331-P302+P352-P304+P340
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Lot numbers can be found on the outside label of a product: