Cas no 33715-53-6 (4-Fluorophenyltriethoxysilane)
4-Fluorophenyltriethoxysilane Chemical and Physical Properties
Names and Identifiers
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- triethoxy(4-fluorophenyl)silane
- 4-Fluorophenyltriethoxysilane
- triethoxy-(4-fluorophenyl)silane
- p-(Fluorophenyl)triethoxysilane
- Benzene, 1-fluoro-4-(triethoxysilyl)-
- DK744
-
- Inchi: 1S/C12H19FO3Si/c1-4-14-17(15-5-2,16-6-3)12-9-7-11(13)8-10-12/h7-10H,4-6H2,1-3H3
- InChI Key: ROIMIGQXVKZRDM-UHFFFAOYSA-N
- SMILES: [Si](C1C=CC(=CC=1)F)(OCC)(OCC)OCC
Computed Properties
- Exact Mass: 258.10874916 g/mol
- Monoisotopic Mass: 258.10874916 g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 17
- Rotatable Bond Count: 7
- Complexity: 191
- 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: 27.7
- Molecular Weight: 258.36
4-Fluorophenyltriethoxysilane Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | P92520-5g |
p-(Fluorophenyl)triethoxysilane |
33715-53-6 | 97% | 5g |
¥1398.0 | 2024-07-19 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1920604-100mg |
Triethoxy(4-fluorophenyl)silane |
33715-53-6 | 95% | 100mg |
¥2184.00 | 2024-05-18 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1920604-250mg |
Triethoxy(4-fluorophenyl)silane |
33715-53-6 | 95% | 250mg |
¥3685.00 | 2024-05-18 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1920604-1g |
Triethoxy(4-fluorophenyl)silane |
33715-53-6 | 95% | 1g |
¥8452.00 | 2024-05-18 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1920604-5g |
Triethoxy(4-fluorophenyl)silane |
33715-53-6 | 95% | 5g |
¥22113.00 | 2024-05-18 |
4-Fluorophenyltriethoxysilane Related Literature
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Zhonghua Xiang,Chuanqi Fang,Sanhua Leng,Dapeng Cao J. Mater. Chem. A, 2014,2, 7662-7665
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Chengbin Yang,Hing Lun Tsang,Pui Man Lau,Ken-Tye Yong,Ho Pui Ho,Siu Kai Kong Analyst, 2017,142, 3579-3587
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3. An all-solid-state imprinted polymer-based potentiometric sensor for determination of bisphenol S?Rongning Liang,Tanji Yin,Ruiqing Yao,Wei Qin RSC Adv., 2016,6, 73308-73312
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Xiaofeng Lin RSC Adv., 2016,6, 9002-9006
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Dhamodaran Manikandan,S. Amirthapandian,I. S. Zhidkov,A. I. Kukharenko,S. O. Cholakh,Ramaswamy Murugan Phys. Chem. Chem. Phys., 2018,20, 6500-6514
Additional information on 4-Fluorophenyltriethoxysilane
4-Fluorophenyltriethoxysilane (CAS No. 33715-53-6): An Overview and Applications in Modern Chemistry
4-Fluorophenyltriethoxysilane (CAS No. 33715-53-6) is a versatile organosilane compound that has gained significant attention in recent years due to its unique properties and wide range of applications in various fields of chemistry, including materials science, pharmaceuticals, and surface modification. This compound is characterized by its molecular structure, which consists of a fluorinated aromatic ring attached to a triethoxysilane group. The combination of these functional groups imparts specific chemical and physical properties that make it an essential reagent in many advanced chemical processes.
The fluorinated aromatic ring in 4-Fluorophenyltriethoxysilane provides enhanced stability and resistance to chemical degradation, making it suitable for use in harsh environments. The triethoxysilane group, on the other hand, is highly reactive and can undergo hydrolysis and condensation reactions to form siloxane bonds, which are crucial for the formation of stable and durable coatings and films. These properties have led to its widespread use in the development of functional materials, such as anti-corrosion coatings, adhesives, and sealants.
In the field of materials science, 4-Fluorophenyltriethoxysilane has been extensively studied for its ability to modify the surface properties of various substrates. Recent research has shown that this compound can significantly improve the hydrophobicity and oleophobicity of surfaces, making it ideal for applications where water and oil repellency are required. For example, a study published in the Journal of Colloid and Interface Science demonstrated that coatings prepared using 4-Fluorophenyltriethoxysilane exhibited excellent water contact angles, indicating superior hydrophobicity.
In the pharmaceutical industry, 4-Fluorophenyltriethoxysilane has found applications in drug delivery systems. The compound's ability to form stable coatings on nanoparticles has been exploited to enhance the stability and bioavailability of drugs. A notable example is the use of 4-Fluorophenyltriethoxysilane-coated silica nanoparticles for the controlled release of anticancer drugs. Research published in the International Journal of Pharmaceutics showed that these nanoparticles exhibited sustained drug release profiles and improved therapeutic efficacy compared to uncoated nanoparticles.
The unique reactivity of 4-Fluorophenyltriethoxysilane also makes it a valuable reagent in organic synthesis. Its ability to undergo various chemical transformations, such as coupling reactions with other functional groups, has been utilized to synthesize complex molecules with tailored properties. For instance, a study in the Tetrahedron Letters reported the successful synthesis of novel fluorinated compounds using 4-Fluorophenyltriethoxysilane as a starting material. These compounds showed promising biological activities and potential applications in medicinal chemistry.
In addition to its applications in materials science and pharmaceuticals, 4-Fluorophenyltriethoxysilane has also been explored for its potential in environmental remediation. The compound's ability to form stable coatings on surfaces can be harnessed to develop materials that can effectively adsorb pollutants from water and air. A recent study published in the Journal of Hazardous Materials demonstrated that 4-Fluorophenyltriethoxysilane-modified silica particles exhibited high adsorption capacities for heavy metals and organic pollutants, making them promising candidates for environmental cleanup technologies.
The synthesis of 4-Fluorophenyltriethoxysilane typically involves the reaction of 4-fluorophenylmagnesium bromide with triethoxychlorosilane followed by hydrolysis and condensation reactions. This process can be optimized to achieve high yields and purity levels, ensuring that the final product meets the stringent requirements of various industrial applications. Recent advancements in synthetic methods have focused on developing more efficient and environmentally friendly routes for the production of this compound.
In conclusion, 4-Fluorophenyltriethoxysilane (CAS No. 33715-53-6) is a multifunctional organosilane compound with a wide range of applications in modern chemistry. Its unique combination of a fluorinated aromatic ring and a reactive triethoxysilane group makes it an essential reagent for surface modification, drug delivery systems, organic synthesis, and environmental remediation. Ongoing research continues to uncover new possibilities for this versatile compound, further expanding its utility in various scientific and industrial fields.
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