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Structure of 19415-51-1
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5-Fluoro-2-methoxybenzaldehyde features a fluorine atom at the para position and a methoxy group at the ortho position relative to the aldehyde, delivering enhanced electron-withdrawing character and improved solubility. This combination enables efficient coupling in transition-metal-catalyzed reactions and facilitates access to complex heterocycles in medicinal chemistry applications.
5-Fluoro-2-methoxybenzaldehyde serves as a versatile building block in medicinal chemistry and materials science, enabling efficient access to substituted aromatic scaffolds. Its ortho-methoxy and meta-fluoro substituents provide complementary reactivity for cross-coupling, electrophilic substitution, and nucleophilic addition reactions. The aldehyde functionality facilitates imine formation, reductive amination, and cyclization processes, while the molecule exhibits excellent bench stability and ease of purification.
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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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: