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Structure of 23605-23-4
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2-Chloro-N-cyclohexylacetamide features a cyclohexyl-amide scaffold with a strategically positioned chloro substituent, delivering enhanced lipophilicity and metabolic stability. This configuration supports efficient integration into bioactive scaffolds and enables selective interactions in medicinal chemistry campaigns.
2-Chloro-N-cyclohexylacetamide serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds and peptide-like motifs. Its chloroacetyl moiety facilitates nucleophilic substitution reactions with amines, thiols, and alcohols under mild conditions, offering high functional group tolerance and reliable yields. The cyclohexyl amide group enhances lipophilicity and metabolic stability, making it valuable for optimizing pharmacokinetic profiles. Bench-stable and readily purified by crystallization or column chromatography, it supports scalable synthesis in both academic and industrial R&D workflows.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H301-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: