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Structure of 6361-23-5
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2,5-Dichlorobenzaldehyde features a rigid aromatic core bearing two chlorine substituents at the 2- and 5-positions, enhancing its electron-deficient character. This configuration supports efficient electrophilic substitution and facilitates incorporation into heterocyclic systems. The aldehyde group enables direct coupling reactions, offering a stable, moisture-tolerant handle for synthetic applications in medicinal chemistry and materials science.
2,5-Dichlorobenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling the construction of heterocyclic scaffolds and functionalized aryl systems. Its ortho-dichloro substitution pattern provides enhanced electrophilicity at the carbonyl center while maintaining bench stability and compatibility with common coupling reactions. The molecule facilitates efficient derivatization via nucleophilic addition, Ullmann-type couplings, and transition-metal-catalyzed transformations, making it valuable for medicinal chemistry and materials science applications.
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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 : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: