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Structure of 60611-22-5
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2-Chloro-6-(trifluoromethyl)benzaldehyde features a trifluoromethyl group that imparts strong electron-withdrawing character, enhancing reactivity in nucleophilic additions. The ortho-chloro substituent provides steric and electronic modulation, while the aldehyde functionality enables direct coupling in synthesis. This compound serves as a key building block for pharmaceutical intermediates and functional materials.
2-Chloro-6-(trifluoromethyl)benzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of biologically relevant heterocycles. Its orthogonal reactivity profile—combining a stable aldehyde functionality with electron-withdrawing chlorine and trifluoromethyl groups—facilitates diverse transformations including nucleophilic additions, Suzuki couplings, and condensation reactions. The compound exhibits excellent bench stability and is readily purified by distillation or recrystallization, supporting scalable synthesis workflows.
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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: