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Structure of 89570-84-3
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2-Hydrazinyl-4-(trifluoromethyl)pyridine features a reactive hydrazino group appended to a trifluoromethyl-substituted pyridine scaffold, enabling efficient coupling in heterocyclic synthesis. The electron-deficient pyridine ring enhances electrophilicity at the C2 position, facilitating nucleophilic addition reactions. This compound serves as a key intermediate for bioactive molecule construction, particularly in medicinal chemistry applications requiring stable, functionalized heterocycles under standard conditions.
2-Hydrazinyl-4-(trifluoromethyl)pyridine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyridine-based pharmacophores. Its hydrazinyl group facilitates cyclization reactions with carbonyl electrophiles, while the trifluoromethyl moiety enhances metabolic stability and lipophilicity. The compound exhibits good bench stability and compatibility with standard synthetic workflows, supporting straightforward purification and integration into multi-step sequences for API intermediate development.
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GHS Pictogram :
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: