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Structure of 93118-03-7
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2-Chloro-3-(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 incorporation into heterocycles and conjugated systems under standard conditions. This compound serves as a key intermediate in pharmaceutical synthesis and materials chemistry.
2-Chloro-3-(trifluoromethyl)benzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of biologically active heterocycles. Its electron-withdrawing trifluoromethyl and ortho-chloro substituents enhance reactivity in nucleophilic additions and condensation reactions. The aldehyde group facilitates straightforward derivatization via imine formation, reductive amination, or Ullmann-type coupling, while the molecule exhibits good bench stability and compatibility with standard purification techniques.
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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: