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Structure of 2646-91-5
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2,3-Difluorobenzaldehyde features a fluorinated aromatic ring with adjacent electron-withdrawing substituents, enhancing its reactivity in nucleophilic addition and transition-metal-catalyzed coupling reactions. This bench-stable aldehyde integrates readily into complex molecular architectures, particularly in medicinal chemistry and agrochemical synthesis.
2,3-Difluorobenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to fluorinated aromatic scaffolds. Its ortho-difluoro substitution pattern enhances metabolic stability and modulates electronic properties, while the aldehyde functionality facilitates diverse transformations including reductive amination, Wittig reactions, and nucleophilic addition. Bench-stable and readily purified by distillation or column chromatography, it functions reliably in standard synthetic workflows.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 1989
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H226-H315-H319-H335
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P370+P378-P405-P501
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Lot numbers can be found on the outside label of a product: