• 1. Ester-directed orthogonal dual C–H activation and ortho aryl C–H alkenylation via distal weak coordination?
  Manickam Bakthadoss,Tadiparthi Thirupathi Reddy,Vishal Agarwal,Duddu S. Sharada Chem. Commun., 2022,58, 1406-1409
• 2. Distinct roles of SNARE-mimicking lipopeptides during initial steps of membrane fusion?
  Alena Koukalová,?árka Pokorná,Aimee L. Boyle,Nestor Lopez Mora,Alexander Kros,Martin Hof,Radek ?achl Nanoscale, 2018,10, 19064-19073
• 3. Excimer and exciplex formation in a pair of bright phosphorescent isomers constructed from Cu3(pyrazolate)3 and Cu3I3 coordination luminophores?
  Shun-Ze Zhan,Mian Li,Xiao-Ping Zhou,Dan Li,Seik Weng Ng RSC Adv., 2011,1, 1457-1459
• 4. Enabling non-flammable Li-metal batteries via electrolyte functionalization and interface engineering?
  Jing Yu,Yu-Qi Lyu,Jiapeng Liu,Mohammed B. Effat,Junxiong Wu J. Mater. Chem. A, 2019,7, 17995-18002
• 5. Fate of single walled carbon nanotubes in wetland ecosystems?
  Joseph H. Bisesi,Tara Sabo-Attwood Environ. Sci.: Nano, 2014,1, 574-583

• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Organonitrogen compounds
• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds

Cyclohexylmethyl Sulfamoyl Chloride: A Comprehensive Overview

Cyclohexylmethyl sulfamoyl chloride, also known by its CAS number 83842-57-3, is a significant compound in the field of organic chemistry. This compound is widely recognized for its versatility and applications in various chemical processes. The cyclohexylmethyl group attached to the sulfamoyl chloride moiety imparts unique properties that make it valuable in both academic research and industrial settings.

Recent studies have highlighted the importance of cyclohexylmethyl sulfamoyl chloride in the synthesis of advanced materials. Researchers have demonstrated its role in the formation of high-performance polymers, where the compound acts as a key intermediate. The ability of cyclohexylmethyl sulfamoyl chloride to undergo nucleophilic substitution reactions has been extensively explored, particularly in the context of developing novel drug delivery systems.

In addition to its role in polymer chemistry, cyclohexylmethyl sulfamoyl chloride has found applications in the pharmaceutical industry. Its use as an intermediate in the synthesis of bioactive compounds has been documented in several recent publications. For instance, a 2023 study published in *Journal of Medicinal Chemistry* utilized this compound to synthesize a new class of anti-inflammatory agents, showcasing its potential in drug discovery.

The synthesis of cyclohexylmethyl sulfamoyl chloride involves a multi-step process that begins with the reaction of cyclohexylmethanol with thionyl chloride. This reaction sequence not only highlights the importance of stoichiometric control but also underscores the need for precise reaction conditions to achieve optimal yields. Recent advancements in catalytic methods have further enhanced the efficiency of this synthesis pathway.

From an environmental perspective, the handling and disposal of cyclohexylmethyl sulfamoyl chloride require careful consideration due to its reactive nature. Studies have shown that proper waste management practices can significantly reduce its environmental footprint. The development of eco-friendly alternatives and recycling methods for this compound is an active area of research.

In conclusion, cyclohexylmethyl sulfamoyl chloride (CAS No: 83842-57-3) stands as a testament to the ingenuity and progress in modern organic chemistry. Its diverse applications, coupled with ongoing research into its synthesis and utilization, ensure that it remains a focal point for scientists and industries alike. As new discoveries emerge, this compound will undoubtedly continue to play a pivotal role in shaping the future of chemical innovation.

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