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Structure of 90390-49-1
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3-Chloro-5-fluorobenzaldehyde features a dual-heteroatom-substituted aromatic ring that imparts enhanced electron deficiency and directional reactivity. This bench-stable aldehyde integrates readily into cross-coupling and condensation reactions, serving as a key building block for pharmaceutical intermediates and functional materials.
3-Chloro-5-fluorobenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of substituted heterocycles and biaryl scaffolds. Its orthogonal halogen functionality facilitates palladium-catalyzed cross-coupling reactions, while the aldehyde group supports imine formation, reductive amination, and nucleophilic addition processes. Bench-stable and compatible with standard purification methods, it functions reliably in multi-step synthetic sequences requiring precise regiocontrol.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: