Cas no 18081-08-8 (2-(Trimethylsilyl)oxynaphthalene)
2-(Trimethylsilyl)oxynaphthalene Chemical and Physical Properties
Names and Identifiers
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- Silane, trimethyl(2-naphthalenyloxy)-
- (2-Naphtyloxy)trimethylsilane
- trimethyl(naphthalen-2-yloxy)silane
- 2-Naphthalenol, TMS ether
- HJWDNWKQENUSKL-UHFFFAOYSA-N
- 2-Naphthol, TMS derivative
- Silane, trimethyl(2-naphthyloxy)-
- 2-trimethylsilyloxynaphtha-lene
- DTXSID50334049
- 18081-08-8
- 2-Trimethylsilyloxynaphthalene
- 2-Naphthyl trimethylsilyl ether
- 2-(Trimethylsiloxy)naphthalene
- 2-[(Trimethylsilyl)oxy]naphthalene
- 2-(Trimethylsilyl)oxynaphthalene
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- Inchi: 1S/C13H16OSi/c1-15(2,3)14-13-9-8-11-6-4-5-7-12(11)10-13/h4-10H,1-3H3
- InChI Key: HJWDNWKQENUSKL-UHFFFAOYSA-N
- SMILES: [Si](C)(C)(C)OC1C=CC2C=CC=CC=2C=1
Computed Properties
- Exact Mass: 216.09708
- Monoisotopic Mass: 216.097041664g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 15
- Rotatable Bond Count: 2
- Complexity: 209
- 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: 9.2?2
Experimental Properties
- PSA: 9.23
- LogP: 4.05350
2-(Trimethylsilyl)oxynaphthalene Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | T787620-500mg |
2-[(Trimethylsilyl)oxy]naphthalene |
18081-08-8 | 500mg |
$230.00 | 2023-05-17 | ||
| TRC | T787620-1g |
2-[(Trimethylsilyl)oxy]naphthalene |
18081-08-8 | 1g |
$ 350.00 | 2022-06-02 | ||
| TRC | T787620-2.5g |
2-[(Trimethylsilyl)oxy]naphthalene |
18081-08-8 | 2.5g |
$ 800.00 | 2023-09-05 | ||
| TRC | T787620-5g |
2-[(Trimethylsilyl)oxy]naphthalene |
18081-08-8 | 5g |
$1728.00 | 2023-05-17 | ||
| TRC | T787620-1000mg |
2-[(Trimethylsilyl)oxy]naphthalene |
18081-08-8 | 1g |
$425.00 | 2023-05-17 |
2-(Trimethylsilyl)oxynaphthalene Related Literature
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Dhirendra K. Chaudhary,Pramendra Kumar,Lokendra Kumar RSC Adv., 2016,6, 94731-94738
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3. Estimating and correcting interference fringes in infrared spectra in infrared hyperspectral imagingGhazal Azarfar,Ebrahim Aboualizadeh,Nicholas M. Walter,Simona Ratti,Camilla Olivieri,Alessandra Norici,Michael Nasse,Achim Kohler,Mario Giordano Analyst, 2018,143, 4674-4683
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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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M. Zeiger,N. J?ckel,P. Strubel,L. Borchardt,R. Reinhold,W. Nickel,J. Eckert,V. Presser,S. Kaskel J. Mater. Chem. A, 2015,3, 17983-17990
Additional information on 2-(Trimethylsilyl)oxynaphthalene
Silane, Trimethyl(2-Naphthalenyloxy)-: A Comprehensive Overview
Silane, specifically trimethyl(2-naphthalenyloxy)silane, is a unique compound with the CAS registry number 18081-08-8. This molecule belongs to the class of organosilicon compounds, characterized by its trimethylsilane core and a naphthol-derived substituent at the oxygen atom. The structure of this compound is highly intriguing due to its combination of aromatic and silicon-based functionalities, making it a subject of interest in various fields including organic chemistry, materials science, and biomedical research.
The compound features a trimethylsilane group, which is known for its stability and ability to participate in various chemical reactions. Additionally, the naphthalenyloxy substituent introduces aromaticity into the molecule, potentially enhancing its reactivity and electronic properties. This duality makes it a versatile building block for constructing complex molecules with diverse applications.
In recent years, there has been growing interest in silicon-containing compounds due to their unique electronic and photonic properties. Research has shown that silanes like trimethyl(2-naphthalenyloxy)silane can act as efficient electron-transport materials in organic light-emitting diodes (OLEDs) and other optoelectronic devices. The naphthalene moiety, being a conjugated aromatic system, contributes to the compound's ability to facilitate charge transport, making it valuable in display technology and photonics.
Moreover, studies have explored the potential of this silane in biomedical applications. Its silicon-oxygen framework is known to be biocompatible, which makes it a promising candidate for drug delivery systems or as a component in bioresorbable materials. The naphthol group could potentially serve as a targeting moiety for specific cellular receptors, opening avenues for tailored therapeutic interventions.
From a synthetic standpoint, trimethyl(2-naphthalenyloxy)silane can be prepared through various methods, including nucleophilic substitution and coupling reactions. Its synthesis is straightforward, making it accessible for researchers in both academic and industrial settings. The compound's stability under ambient conditions further enhances its suitability for large-scale production and application.
Recent advancements in nanotechnology have also highlighted the potential of silanes like trimethyl(2-naphthalenyloxy)silane as building blocks for constructing silicon-based nanoparticles. These nanoparticles could be used in imaging, sensing, and therapy, leveraging both the silicon's biocompatibility and the naphthol group's specific binding properties.
In conclusion, trimethyl(2-naphthalenyloxy)silane is a multifaceted compound with applications spanning materials science, photonics, and biomedical engineering. Its unique combination of functionalities positions it as a valuable tool for researchers seeking to develop innovative solutions in these fields. As research into silicon-based materials continues to evolve, compounds like this silane are likely to play an increasingly important role in advancing technology and medicine.
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