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Structure of 1023813-33-3
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6-Methyl-5-(trifluoromethyl)pyridin-2-amine features a trifluoromethyl group that imparts enhanced electron-withdrawal and metabolic stability, while the methyl substituent fine-tunes electronic properties. This pyridine scaffold serves as a key building block in medicinal chemistry, particularly for kinase inhibitors and bioactive heterocycles.
6-Methyl-5-(trifluoromethyl)pyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through palladium-catalyzed cross-coupling and electrophilic substitution reactions. Its electron-deficient pyridine core exhibits favorable reactivity in C–H functionalization and Suzuki-Miyaura coupling, while the methyl and trifluoromethyl groups provide steric and electronic modulation. The compound demonstrates bench stability and compatibility with standard purification protocols, facilitating integration into multi-step synthetic sequences for drug discovery applications.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: