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Structure of 103426-20-6
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3-Chloro-5-methylbenzaldehyde features a benzaldehyde core with electron-withdrawing chlorine and electron-donating methyl groups in meta and para positions relative to the aldehyde. This substitution pattern imparts enhanced reactivity in nucleophilic addition reactions while maintaining bench-stable handling characteristics. The compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and functionalized heterocycles.
3-Chloro-5-methylbenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of substituted aromatic scaffolds. Its ortho-chloro and meta-methyl substituents provide predictable electronic and steric modulation, enhancing reactivity in nucleophilic additions, Grignard couplings, and Ullmann-type transformations. The aldehyde functionality offers high compatibility with standard functional group manipulations, including reductive amination and Wittig reactions. Bench-stable and readily purified by distillation or recrystallization, it supports scalable synthesis workflows with consistent yields across diverse reaction conditions.
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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: