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Structure of 19342-88-2
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3-Chloro-N-(p-tolyl)propanamide features a chlorinated aliphatic chain linked to a para-tolyl-substituted amide, combining enhanced lipophilicity with steric bulk. This structural motif enables robust integration into bioactive scaffolds, particularly in kinase inhibitor design and medicinal chemistry lead optimization. The molecule exhibits favorable stability under standard bench conditions and facilitates efficient coupling in multistep synthetic sequences.
3-Chloro-N-(p-tolyl)propanamide serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles and pharmaceutical intermediates. Its chloro-substituted aliphatic amide functionality offers predictable reactivity in nucleophilic substitution and coupling reactions, with good bench stability and straightforward purification via recrystallization or chromatography.
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Lot numbers can be found on the outside label of a product: