• 1. Establishing empirical design rules of nucleic acid templates for the synthesis of silver nanoclusters with tunable photoluminescence and functionalities towards targeted bioimaging applications?
  Jason Y. C. Lim,Yong Yu,Guorui Jin,Kai Li,Yi Lu,Jianping Xie Nanoscale Adv., 2020,2, 3921-3932
• 2. Emerging investigator series: bacteriophages as nano engineering tools for quality monitoring and pathogen detection in water and wastewater
  Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
• 3. Excitable dynamics in the bromate–sulfite–ferrocyanide reaction
  J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
• 4. Excimer and exciplex formation in a pair of bright phosphorescent isomers constructed from Cu3(pyrazolate)3 and Cu3I3 coordination luminophores?
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• 5. Establishment and implications of a characterization method for magnetic nanoparticle using cell tracking velocimetry and magnetic susceptibility modified solutions
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• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Secondary alcohols
• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Alcohols and polyols Secondary alcohols
• Solvents and Organic Chemicals Organic Compounds Alcohol/Ether

Comprehensive Overview of 3-Aminocyclohexanol Hydrochloride (CAS No. 1263378-29-5): Properties, Applications, and Research Insights

3-Aminocyclohexanol hydrochloride (CAS No. 1263378-29-5) is a versatile organic compound with significant relevance in pharmaceutical and chemical research. This white crystalline powder, characterized by its cyclohexane backbone and amine functional group, has garnered attention for its potential in drug synthesis and material science. The hydrochloride salt form enhances its stability and solubility, making it a preferred choice for laboratory applications.

In recent years, the demand for high-purity aminocyclohexanol derivatives has surged, driven by advancements in small-molecule therapeutics and catalysis research. Researchers frequently search for "3-Aminocyclohexanol hydrochloride solubility" or "CAS 1263378-29-5 synthesis method," reflecting its technical importance. The compound’s unique stereochemistry also positions it as a key intermediate in designing chiral catalysts, a hot topic in green chemistry.

From a structural perspective, the cyclohexanol ring provides rigidity, while the amine group offers reactivity for further modifications. This dual functionality explains its utility in creating bioactive scaffolds, a trending focus in medicinal chemistry. Notably, its applications extend to peptide mimetics and polymer precursors, aligning with industry shifts toward sustainable materials.

Quality control of 3-Aminocyclohexanol HCl (CAS 1263378-29-5) often involves HPLC and NMR analysis, addressing common queries like "how to verify 3-Aminocyclohexanol purity." Storage recommendations typically emphasize protection from moisture, as the compound’s hygroscopic nature is a critical handling consideration. These practical insights are vital for laboratories optimizing high-yield reactions.

Emerging studies explore its role in neurotransmitter analogs, tapping into the growing interest in CNS-targeted compounds. While not a standalone drug, its structural motifs appear in patents for neurological disorder treatments—a sector experiencing rapid growth. This connection to neuroscience research enhances its profile beyond traditional synthetic uses.

Environmental considerations are also shaping its applications. The compound’s potential in biodegradable chelating agents resonates with searches for "eco-friendly amine derivatives." Such developments highlight how CAS 1263378-29-5 intersects with sustainability trends, a priority for modern chemical enterprises.

In summary, 3-Aminocyclohexanol hydrochloride exemplifies the intersection of fundamental chemistry and applied science. Its adaptability across domains—from pharmaceutical intermediates to advanced material design—ensures continued relevance. As research evolves, so too will innovative uses for this multifaceted compound, solidifying its place in the scientific toolkit.

• 50910-54-8(trans-4-aminocyclohexanol;hydrochloride)
• 56239-26-0(cis-4-aminocyclohexan-1-ol hydrochloride)
• 721884-82-8((1R,3R)-3-aminocyclohexanol)
• 1110772-22-9((1R,3S)-3-Aminocyclohexanol)
• 1110772-04-7((1S,3R)-3-AMINOCYCLOHEXANOL)
• 6982-42-9(cis-3-aminocyclohexanol)
• 6850-39-1(3-Aminocyclohexanol)
• 40525-77-7(trans-3-aminocyclohexanol)
• 76445-65-3(4-aminocyclohexan-1-ol hydrochloride)
• 721884-81-7((1S,3S)-3-aminocyclohexanol)