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Structure of 1603584-72-0
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4-Bromo-5-chloro-2-fluorobenzaldehyde features a trifluorinated aromatic core with strategically positioned halogens, enabling direct coupling in cross-coupling reactions. The aldehyde group provides a reactive handle for nucleophilic addition or condensation chemistry, while the electron-deficient ring enhances electrophilicity for downstream functionalization. This compound serves as a key building block in pharmaceutical intermediates and advanced materials synthesis.
4-Bromo-5-chloro-2-fluorobenzaldehyde serves as a versatile electrophilic building block in medicinal chemistry and materials science, enabling direct incorporation of halogenated aromatic motifs into complex molecular architectures. Its trifunctional substitution pattern—bromine, chlorine, and fluorine—confers enhanced metabolic stability and modulates electronic properties, while the aldehyde group facilitates nucleophilic additions, imine formations, and downstream functionalization. Bench-stable and compatible with standard cross-coupling protocols (e.g., Suzuki, Stille), it functions efficiently in late-stage diversification and heterocycle synthesis.
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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: