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Structure of 369-25-5
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Methyl 3,4-difluorobenzoate features a fluorinated aromatic core with strategically positioned electron-withdrawing substituents. This bench-stable ester integrates readily into synthetic sequences requiring polar, electron-deficient aryl handles. The para-fluorine enhances metabolic stability in bioactive molecule design, while the methyl ester enables facile derivatization under standard conditions.
Methyl 3,4-difluorobenzoate serves as a versatile building block in medicinal chemistry and synthetic organic chemistry. The ortho-difluoro substitution pattern enhances metabolic stability and modulates electronic properties, while the ester functionality enables straightforward derivatization via hydrolysis, reduction, or coupling reactions. Its bench-stable nature and compatibility with palladium-catalyzed cross-coupling processes make it a practical choice for constructing complex heterocyclic scaffolds and drug-like molecules.
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1325
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Class : 4.1
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-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: