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Structure of 1056162-06-1
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This trifluoromethylpyridylmethanamine features a pyridine ring bearing a trifluoromethyl group and a primary amine at the adjacent position, enabling direct integration into pharmaceutical scaffolds. The electron-deficient aromatic system enhances reactivity in cross-coupling and functionalization processes.
(2-(Trifluoromethyl)pyridin-3-yl)methanamine serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through nucleophilic substitution and coupling reactions. Its trifluoromethylpyridine core provides enhanced metabolic stability and modulated lipophilicity, while the primary amine functionality facilitates straightforward derivatization. The compound exhibits good bench stability and is compatible with standard synthetic workflows, making it a practical choice for API intermediate development and structure–activity studies.
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GHS Pictogram :
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GHS No : GHS02,GHS05
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Signal Word : Danger
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UN#: 1993
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H226-H314
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P280-P303+P361+P353-P370+P378-P403+P235-P501
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Lot numbers can be found on the outside label of a product: