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Structure of 869108-35-0
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Methyl 3-fluoropicolinate features a fluorinated pyridine ring enabling enhanced electronic effects in synthetic transformations. The ester functionality supports direct derivatization, while the ortho-fluorine imparts metabolic stability and improved binding affinity in medicinal chemistry applications. This bench-stable compound integrates readily into diverse reaction sequences under standard conditions.
Methyl 3-fluoropicolinate serves as a versatile building block in medicinal chemistry, enabling efficient construction of fluorinated heterocycles and bioactive scaffolds. Its electron-deficient pyridine core facilitates nucleophilic substitution and transition-metal-catalyzed coupling reactions. The methyl ester group offers convenient derivatization options, while the 3-fluoro substituent provides enhanced metabolic stability and targeted binding interactions in drug discovery applications. Bench-stable and compatible with standard purification protocols, it functions reliably in multistep syntheses.
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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: