Cas no 1217863-49-4 (2-(Dimethyl-naphthalen-1-yl-silanyl)-phenyl-methanol)

2-(Dimethyl-naphthalen-1-yl-silanyl)-phenyl-methanol is a silanol-containing aromatic alcohol with a naphthalene backbone, offering unique reactivity due to the combination of silicon and hydroxyl functional groups. The dimethylsilanyl moiety enhances stability while allowing for selective transformations, making it useful in organosilicon chemistry and cross-coupling reactions. The naphthalene group provides steric bulk and electronic effects, influencing regioselectivity in synthetic applications. This compound is particularly valuable as an intermediate in the synthesis of advanced materials, ligands, or pharmaceuticals, where controlled functionalization is required. Its hybrid structure enables compatibility with both organic and organometallic reaction conditions, broadening its utility in research and industrial processes.
2-(Dimethyl-naphthalen-1-yl-silanyl)-phenyl-methanol structure
1217863-49-4 structure
Product Name:2-(Dimethyl-naphthalen-1-yl-silanyl)-phenyl-methanol
CAS No:1217863-49-4
MF:C19H20OSi
MW:292.447006225586
MDL:MFCD16251548
CID:1073425
PubChem ID:57416882
Update Time:2025-08-02

2-(Dimethyl-naphthalen-1-yl-silanyl)-phenyl-methanol Chemical and Physical Properties

Names and Identifiers

    • {2-[Dimethyl(naphthalen-1-yl)silyl]phenyl}methanol
    • 2-[Dimethyl(1-naphthyl)silyl]benzyl alcohol
    • [2-[dimethyl(naphthalen-1-yl)silyl]phenyl]methanol
    • AKOS025392274
    • (2-(Dimethyl(naphthalen-1-yl)silyl)phenyl)methanol
    • CS-0334922
    • [2-(Dimethyl-naphthalen-1-yl-silanyl)-phenyl]-methanol
    • DTXSID90726227
    • 1217863-49-4
    • AS-2229
    • A927198
    • MFCD16251548
    • 2-(Dimethyl-naphthalen-1-yl-silanyl)-phenyl-methanol
    • MDL: MFCD16251548
    • Inchi: 1S/C19H20OSi/c1-21(2,18-12-6-4-9-16(18)14-20)19-13-7-10-15-8-3-5-11-17(15)19/h3-13,20H,14H2,1-2H3
    • InChI Key: QYFMWBREKHLBGO-UHFFFAOYSA-N
    • SMILES: [Si](C)(C)(C1C=CC=CC=1CO)C1=CC=CC2C=CC=CC1=2

Computed Properties

  • Exact Mass: 292.128341792g/mol
  • Monoisotopic Mass: 292.128341792g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 21
  • Rotatable Bond Count: 3
  • Complexity: 341
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 20.2?2

2-(Dimethyl-naphthalen-1-yl-silanyl)-phenyl-methanol Security Information

2-(Dimethyl-naphthalen-1-yl-silanyl)-phenyl-methanol Pricemore >>

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abcr
AB264335-1 g
2-[Dimethyl(1-naphthyl)silyl]benzyl alcohol, 95%; .
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abcr
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Additional information on 2-(Dimethyl-naphthalen-1-yl-silanyl)-phenyl-methanol

Recent Advances in the Study of 2-(Dimethyl-naphthalen-1-yl-silanyl)-phenyl-methanol (CAS: 1217863-49-4)

In recent years, the compound 2-(Dimethyl-naphthalen-1-yl-silanyl)-phenyl-methanol (CAS: 1217863-49-4) has garnered significant attention in the field of chemical biology and pharmaceutical research. This organosilicon compound, characterized by its unique structural features, has shown promising potential in various applications, including drug development, material science, and catalytic processes. The integration of silicon into organic frameworks, as exemplified by this compound, offers distinct advantages such as enhanced stability, tunable reactivity, and novel pharmacological properties. This research brief aims to provide an overview of the latest findings related to this compound, highlighting its synthesis, characterization, and potential applications.

The synthesis of 2-(Dimethyl-naphthalen-1-yl-silanyl)-phenyl-methanol involves a series of well-defined chemical transformations, typically starting from naphthalene derivatives and silicon-containing precursors. Recent studies have focused on optimizing the synthetic routes to improve yield and purity, with particular emphasis on green chemistry principles to minimize environmental impact. Advanced spectroscopic techniques, including nuclear magnetic resonance (NMR) and mass spectrometry (MS), have been employed to confirm the structural integrity of the compound. Additionally, X-ray crystallography has provided valuable insights into its three-dimensional conformation, which is critical for understanding its interaction with biological targets.

One of the most exciting developments in the study of 2-(Dimethyl-naphthalen-1-yl-silanyl)-phenyl-methanol is its potential as a bioactive molecule. Preliminary in vitro and in vivo studies have demonstrated its ability to modulate specific biochemical pathways, making it a candidate for further investigation in therapeutic applications. For instance, its interaction with certain enzymes and receptors suggests possible utility in treating inflammatory and neurodegenerative diseases. Furthermore, the compound's unique electronic properties have sparked interest in its use as a building block for advanced materials, such as organic semiconductors and luminescent probes.

Despite these promising findings, challenges remain in the development and application of 2-(Dimethyl-naphthalen-1-yl-silanyl)-phenyl-methanol. Issues such as scalability of synthesis, bioavailability, and long-term stability need to be addressed to fully realize its potential. Ongoing research is exploring various strategies to overcome these hurdles, including the development of novel derivatives and formulation techniques. Collaborative efforts between academia and industry are expected to accelerate progress in this area, paving the way for innovative solutions in drug discovery and material science.

In conclusion, 2-(Dimethyl-naphthalen-1-yl-silanyl)-phenyl-methanol represents a fascinating example of how organosilicon chemistry can contribute to advancements in chemical biology and pharmaceuticals. The compound's versatile properties and broad applicability underscore its importance as a subject of ongoing research. As new findings continue to emerge, it is anticipated that this compound will play an increasingly prominent role in addressing some of the most pressing challenges in the field. Future studies should focus on elucidating its mechanism of action, optimizing its pharmacological profile, and exploring its potential in interdisciplinary applications.

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