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Structure of 1227499-99-1
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2-Chloro-4-methoxy-5-(trifluoromethyl)pyridine features a trifluoromethyl group that enhances electron-withdrawal and metabolic stability, while the methoxy substituent improves solubility and reactivity in cross-coupling processes. This pyridine scaffold serves as a key building block in agrochemical and pharmaceutical synthesis, offering robust performance under standard reaction conditions.
2-Chloro-4-methoxy-5-(trifluoromethyl)pyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its reactive C–Cl bond and electron-deficient pyridine core. The methoxy and trifluoromethyl groups provide orthogonal functional handles and enhanced metabolic stability, while the compound exhibits excellent bench stability and compatibility with standard purification methods.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: