• 1. Fatty acid positional distribution in colostrum and mature milk of women living in Inner Mongolia, North Jiangsu and Guangxi of China?
  Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
• 2. Fast-Track to Research Data Management in Experimental Material Science-Setting the Ground for Research Group Level Materials Digitalization.
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• 3. Emerging investigators
  Polym. Chem., 2015,6, 5501-5502
• 4. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?
  Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198
• 5. Ester-mediated peptide formation promoted by deep eutectic solvents: a facile pathway to proto-peptides?
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Comprehensive Overview of 4-(1-methylcyclohexyl)-1,3-thiazol-2-amine (CAS No. 867286-06-4): Properties, Applications, and Industry Insights

The compound 4-(1-methylcyclohexyl)-1,3-thiazol-2-amine (CAS No. 867286-06-4) is a specialized organic molecule featuring a unique thiazole core substituted with a methylcyclohexyl group. This structural configuration endows it with distinct chemical properties, making it a subject of interest in pharmaceutical research, agrochemical development, and material science. Its amine functionality and heterocyclic architecture contribute to its versatility in synthetic applications, particularly in the design of bioactive compounds.

In recent years, the demand for thiazole derivatives has surged due to their prominence in drug discovery. Researchers frequently explore 4-(1-methylcyclohexyl)-1,3-thiazol-2-amine as a potential intermediate for kinase inhibitors or antimicrobial agents, aligning with trends in personalized medicine and antibiotic resistance. The compound’s lipophilic nature, attributed to the methylcyclohexyl moiety, enhances membrane permeability—a critical factor in optimizing drug bioavailability.

From an industrial perspective, CAS 867286-06-4 is often discussed in forums focusing on high-value fine chemicals. Its synthesis typically involves cyclocondensation reactions or catalytic amination, with yields optimized through green chemistry principles. Environmental concerns have driven innovations in solvent-free protocols, resonating with the sustainability mandates of modern chemical manufacturing. Analytical techniques like HPLC and NMR are employed to validate purity, ensuring compliance with regulatory standards such as ICH Q7.

The compound’s nomenclature often intersects with search queries like "thiazole amine synthesis" or "methylcyclohexyl-thiazole applications," reflecting user interest in its synthetic pathways. Additionally, its potential role in crop protection formulations has garnered attention, as agrochemical companies seek novel pesticide adjuvants with lower ecological impact. Patent literature highlights derivatives of 4-(1-methylcyclohexyl)-1,3-thiazol-2-amine as key components in next-generation fungicides.

Quality control for 867286-06-4 remains a priority, with suppliers emphasizing batch-to-batch consistency and traceability. This aligns with the pharmaceutical industry’s shift toward QbD (Quality by Design) frameworks. Furthermore, computational studies leveraging AI-driven molecular modeling have accelerated the exploration of this compound’s structure-activity relationships, reducing R&D timelines.

In summary, 4-(1-methylcyclohexyl)-1,3-thiazol-2-amine exemplifies the intersection of innovation and practicality in modern chemistry. Its multifaceted applications—from drug development to sustainable agriculture—underscore its relevance in addressing global challenges. As research progresses, this compound is poised to play a pivotal role in advancing precision therapeutics and eco-friendly agrochemicals.

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