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Structure of 177756-62-6
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3-Fluoro-4-methylbenzaldehyde features a fluorinated aromatic ring paired with a methyl group and aldehyde functionality, enabling selective coupling reactions in pharmaceutical synthesis. This electron-deficient aldehyde integrates readily into complex scaffolds under standard conditions.
3-Fluoro-4-methylbenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted benzimidazoles, arylamines, and heterocyclic scaffolds. Its fluorinated aromatic ring enhances metabolic stability and modulates electronic properties, while the aldehyde functionality facilitates condensation reactions, reductive amination, and Ullmann-type couplings. Bench-stable and compatible with common protecting group strategies, it offers predictable reactivity in multi-step 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: