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Structure of 697739-03-0
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Methyl 5-fluoro-2-methyl-3-nitrobenzoate features a trifunctional aromatic core with orthogonal reactivity. The electron-deficient ring supports efficient nucleophilic substitution, while the methyl and nitro groups enable selective derivatization. This bench-stable ester integrates readily into synthetic sequences requiring fluorinated building blocks.
Methyl 5-fluoro-2-methyl-3-nitrobenzoate serves as a versatile building block in medicinal chemistry, enabling the synthesis of fluorinated heterocycles and bioactive scaffolds. Its electron-deficient aromatic core facilitates nucleophilic substitution reactions, while the nitro and ester groups offer orthogonal reactivity for downstream functionalization. Bench-stable and readily purified, it supports scalable synthesis workflows in API 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: