• 1. Excellent energy storage performance in NaNbO3-based relaxor antiferroeic ceramics under a low electric field
  XuxinCheng,XiaomingChen,PengyuanFan
• 2. 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
• 3. Evidence that the availability of an allylic hydrogen governs the regioselectivity of the Wacker oxidation
  Matthew J. Gaunt,Jinquan Yu,Jonathan B. Spencer Chem. Commun., 2001, 1844-1845
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  Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
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• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Cyclohexylamines

N-[(1r,4r)-4-methylcyclohexyl]oxan-4-amine: A Comprehensive Overview

N-[(1r,4r)-4-methylcyclohexyl]oxan-4-amine, also known by its CAS number 1592575-28-4, is a compound of significant interest in the fields of organic chemistry and pharmacology. This compound is characterized by its unique structure, which combines a cyclohexane ring with an oxazolidinone moiety. The molecule's stereochemistry plays a crucial role in its biological activity and synthetic applications.

The synthesis of N-[(1r,4r)-4-methylcyclohexyl]oxan-4-amine involves a multi-step process that typically begins with the preparation of the cyclohexane derivative. Recent advancements in asymmetric synthesis have enabled the efficient construction of the (1r,4r) configuration, which is essential for the compound's desired properties. The use of chiral catalysts and enantioselective reactions has significantly improved the yield and enantiomeric purity of this compound.

One of the most promising applications of N-[(1r,4r)-4-methylcyclohexyl]oxan-4-amine lies in its potential as a building block for drug development. The compound's ability to form stable amide bonds makes it an ideal candidate for constructing bioactive molecules. Recent studies have demonstrated its utility in the synthesis of peptide mimetics and small molecule inhibitors targeting various disease pathways.

In addition to its pharmacological applications, N-[(1r,4r)-4-methylcyclohexyl]oxan-4-amine has shown potential in materials science. Its rigid structure and ability to form hydrogen bonds make it suitable for use in supramolecular chemistry and crystal engineering. Researchers have explored its role in creating self-assembled materials with unique mechanical and optical properties.

The latest research on CAS 1592575-28-4 has focused on understanding its interaction with biological systems. Studies using advanced spectroscopic techniques have provided insights into its binding affinity with proteins and nucleic acids. These findings have opened new avenues for exploring its role in gene regulation and enzyme inhibition.

Moreover, the environmental impact of N-[(1r,4r)-4-methylcyclohexyl]oxan-4-amine has been a topic of recent investigation. Researchers have assessed its biodegradability and toxicity profiles under various conditions. These studies are crucial for ensuring the sustainable use of this compound in industrial and pharmaceutical settings.

In conclusion, N-[(1r,4r)-4-methylcyclohexyl]oxan-4-amine (CAS 1592575-28-4) is a versatile compound with diverse applications across multiple disciplines. Its unique structure, combined with recent advancements in synthetic methods and biological studies, positions it as a valuable tool for future innovations in chemistry and medicine.

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