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Structure of 1071435-62-5
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(S)-1-(6-(trifluoromethyl)pyridin-3-yl)ethan-1-amine features a chiral ethylamine side chain attached to a trifluoromethyl-substituted pyridine ring, delivering enhanced electronic and steric properties. This configuration enables precise molecular recognition in asymmetric synthesis, serving as a key scaffold for bioactive molecule construction. The compound exhibits robust bench stability and compatibility with diverse reaction conditions.
(S)-1-(6-(Trifluoromethyl)pyridin-3-yl)ethan-1-amine serves as a versatile chiral building block for medicinal chemistry, enabling the construction of pyridine-containing scaffolds prevalent in pharmaceuticals. Its trifluoromethyl group enhances metabolic stability and lipophilicity, while the chiral amine functionality facilitates stereoselective transformations. The compound exhibits good bench stability and compatibility with standard coupling reactions, simplifying purification and integration into multi-step syntheses.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H315-H318-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: