TCI C0685 Cyclohexanecarbonyl Chloride is a reactive acyl chloride widely used as an acylating reagent in organic synthesis laboratories. It readily reacts with amines, alcohols, and other nucleophiles to form the corresponding amides and esters under mild conditions. Researchers commonly employ it to introduce the cyclohexanecarbonyl moiety into target molecules during building block and early-stage medicinal chemistry work. AMI Scientific offers this TCI product in several package sizes so laboratories can match their working scale, and users should always consult the official label and SDS before handling.
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- Urove et al. (1993). Electrochemical Reduction of Cyclohexanecarbonyl Chloride at Mercury Cathodes in Acetonitrile. Journal of The Electrochemical Society doi:10.1149/1.2056230
- Bhattacharya et al. (1998). Catalytic reduction of cyclohexanecarbonyl chloride with electrogenerated nickel(I) salen in acetonitrile. Journal of Electroanalytical Chemistry doi:10.1016/s0022-0728(97)00418-x
- Akasaka et al. (2006). Chiral discrimination of primary amines by HPLC after labeling with a chiral derivatization reagent, trans‐2‐(2,3‐anthracenedicarboximido)‐cyclohexanecarbonyl chloride. Journal of Separation Science doi:10.1002/jssc.200600025
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