Cas no 25910-98-9 (2-cyclohexyl-2-methyloxirane)

2-Cyclohexyl-2-methyloxirane is a cyclic ether compound characterized by a three-membered oxirane ring substituted with a cyclohexyl and a methyl group. This epoxide is of interest in synthetic organic chemistry due to its reactivity in ring-opening reactions, which enables the formation of diverse functionalized intermediates. The steric and electronic properties imparted by the cyclohexyl moiety influence its selectivity in nucleophilic or electrophilic addition reactions. It serves as a versatile building block for the synthesis of complex molecules, including pharmaceuticals and agrochemicals. The compound’s stability under controlled conditions facilitates handling and storage, making it suitable for laboratory and industrial applications requiring precise epoxide reactivity.
2-cyclohexyl-2-methyloxirane structure
2-cyclohexyl-2-methyloxirane structure
Product Name:2-cyclohexyl-2-methyloxirane
CAS No:25910-98-9
MF:C9H16O
MW:140.222743034363
CID:2134187
PubChem ID:20469406
Update Time:2025-08-04

2-cyclohexyl-2-methyloxirane Chemical and Physical Properties

Names and Identifiers

    • 2-cyclohexyl-2-methylOxirane
    • 2-Methyl-2-cyclohexyloxirane
    • VTBARQXSMYZCEX-UHFFFAOYSA-N
    • racemic 2-cyclohexyl-2-methyloxirane
    • 2-cyclohexyl-2-methyloxirane
    • Inchi: 1S/C9H16O/c1-9(7-10-9)8-5-3-2-4-6-8/h8H,2-7H2,1H3
    • InChI Key: VTBARQXSMYZCEX-UHFFFAOYSA-N
    • SMILES: O1CC1(C)C1CCCCC1

Computed Properties

  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 127
  • Topological Polar Surface Area: 12.5

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2-cyclohexyl-2-methyloxirane Related Literature

Additional information on 2-cyclohexyl-2-methyloxirane

Professional Introduction to Compound with CAS No. 25910-98-9 and Product Name: 2-cyclohexyl-2-methyloxirane

2-cyclohexyl-2-methyloxirane, identified by its Chemical Abstracts Service (CAS) number 25910-98-9, is a significant compound in the realm of organic chemistry and pharmaceutical research. This oxirane derivative, characterized by its cyclohexyl and methyl substituents, has garnered attention due to its versatile applications in synthetic chemistry and potential utility in the development of novel bioactive molecules.

The structure of 2-cyclohexyl-2-methyloxirane consists of a three-membered epoxide ring fused with a cyclohexane moiety, further substituted with a methyl group at the reactive carbon atom. This configuration imparts unique reactivity, making it a valuable intermediate in various chemical transformations. The compound's stability under standard conditions, coupled with its ability to undergo ring-opening reactions, positions it as a promising candidate for further functionalization.

In recent years, the pharmaceutical industry has shown increasing interest in oxirane derivatives due to their broad spectrum of biological activities. 2-cyclohexyl-2-methyloxirane has been explored as a precursor in the synthesis of pharmacologically relevant compounds. Its ability to participate in nucleophilic ring-opening reactions allows for the introduction of diverse functional groups, facilitating the development of molecules with targeted therapeutic effects.

One of the most compelling aspects of 2-cyclohexyl-2-methyloxirane is its potential application in medicinal chemistry. Researchers have leveraged its reactivity to create novel analogs of known drugs, aiming to enhance efficacy and reduce side effects. For instance, studies have demonstrated its utility in generating derivatives with anti-inflammatory and antimicrobial properties. These findings underscore the compound's significance as a building block in drug discovery.

The synthetic methodologies involving 2-cyclohexyl-2-methyloxirane have been refined through continuous innovation. Recent advancements in catalytic systems have enabled more efficient and selective transformations, improving yields and purity. Such improvements are crucial for large-scale production and commercialization of pharmaceuticals derived from this compound.

Moreover, the environmental impact of synthesizing 2-cyclohexyl-2-methyloxirane has been a focus of research. Green chemistry principles have been applied to develop more sustainable synthetic routes, minimizing waste and reducing energy consumption. These efforts align with global initiatives to promote eco-friendly chemical processes, ensuring that the production of this compound remains environmentally responsible.

The role of 2-cyclohexyl-2-methyloxirane extends beyond pharmaceutical applications. It has found utility in materials science, particularly in the development of polymers and coatings. The reactivity of its epoxide ring allows for cross-linking reactions, resulting in materials with enhanced mechanical properties and durability. This dual functionality as both a pharmaceutical intermediate and a material science precursor highlights its versatility.

Recent studies have also explored the potential use of 2-cyclohexyl-2-methyloxirane in agrochemical formulations. Its structural features make it a suitable candidate for synthesizing compounds that exhibit herbicidal or pesticidal activity. By modifying its molecular framework, researchers aim to develop environmentally benign alternatives to conventional agrochemicals, supporting sustainable agriculture practices.

The future prospects for 25910-98-9 are promising, with ongoing research uncovering new applications and refining existing ones. As our understanding of organic chemistry evolves, so does the potential for innovative uses of this compound. Collaborative efforts between academia and industry are essential to translate these findings into tangible benefits for society.

In conclusion, 2-cyclohexyl-2-methyloxirane stands as a testament to the ingenuity of modern chemistry. Its unique properties and broad applicability make it a cornerstone in various fields, from drug development to advanced materials. As research continues to uncover new possibilities, this compound will undoubtedly play an increasingly pivotal role in shaping the future of chemical innovation.

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