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Structure of 1163287-01-1
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Methyl 4-fluoro-2-methyl-5-nitrobenzoate features a fluorinated aromatic core with strategically positioned methyl and nitro groups, enabling selective functionalization in synthetic sequences. The ester moiety offers stable handling under standard conditions while the electron-deficient ring facilitates nucleophilic substitution reactions. This compound serves as a key intermediate in the synthesis of bioactive molecules and advanced materials.
Methyl 4-fluoro-2-methyl-5-nitrobenzoate serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling selective functionalization at the electron-deficient aromatic ring. The fluorine and nitro groups enhance reactivity in nucleophilic substitution and facilitate downstream coupling reactions. Its bench-stable nature and compatibility with standard purification methods make it well-suited for multi-step synthetic sequences.
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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: