Cas no 20083-34-5 (Pentafluorophenyltriethoxysilane)
Pentafluorophenyltriethoxysilane Chemical and Physical Properties
Names and Identifiers
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- Benzene,1,2,3,4,5-pentafluoro-6-(triethoxysilyl)-
- Triethoxy(pentafluorophenyl)silane
- (Pentafluorophenyl)triethoxysilane
- Pentafluorophenyl(triethoxy)silane
- PENTAFLUOROPHENYLTRIETHOXYSILANE
- triethoxy-(2,3,4,5,6-pentafluorophenyl)silane
- (EtO)3SiC6F5
- (Pentafluorphenyl)-triethoxysilan
- [Tris(ethoxy)silyl]perfluorobenzene
- pentafluorophenylethoxysilane
- Pentafluorphenyl-triaethoxysilan
- triethoxy-pentafluorophenyl-silane
- SIP 6716.7
- TRIETHOXY(2,3,4,5,6-PENTAFLUOROPHENYL)SILANE
- A814226
- DTXSID90382180
- MFCD03411257
- AKOS004115289
- FS-4681
- triethoxy-(1,2,3,4,5,6-hexafluorocyclohexa-2,4-dien-1-yl)silane
- Benzene, 1,2,3,4,5-pentafluoro-6-(triethoxysilyl)-
- (Pentafluorophenyl)triethoxysilane, 97%
- T72036
- SCHEMBL231689
- triethoxy(perfluorophenyl)silane
- 20083-34-5
- T3134
- 1,3,3,3-pentamethyldisiloxane
- Pentafluorophenyltriethoxysilane
-
- MDL: MFCD03411257
- Inchi: 1S/C12H15F5O3Si/c1-4-18-21(19-5-2,20-6-3)12-10(16)8(14)7(13)9(15)11(12)17/h4-6H2,1-3H3
- InChI Key: QALDFNLNVLQDSP-UHFFFAOYSA-N
- SMILES: [Si](C1C(=C(C(=C(C=1F)F)F)F)F)(OCC)(OCC)OCC
Computed Properties
- Exact Mass: 330.07100
- Monoisotopic Mass: 330.071
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 21
- Rotatable Bond Count: 7
- Complexity: 292
- 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: 27.7A^2
Experimental Properties
- Color/Form: liquid
- Density: 1.24 g/cm3
- Boiling Point: 238°C(lit.)
- Flash Point: 102.2±27.3 oC,
- Refractive Index: 1.4180
- Solubility: Almost insoluble (0.086 g/l) (25 o C),
- PSA: 27.69000
- LogP: 2.63750
- Solubility: Not determined
- Vapor Pressure: 0.0±0.5 mmHg at 25°C
Pentafluorophenyltriethoxysilane Security Information
-
Symbol:
- Prompt:warning
- Signal Word:warning
- Hazard Statement: H315-H319
- Warning Statement: P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
- WGK Germany:3
- Hazard Category Code: 36/37/38
- Safety Instruction: S26; S36/37/39
-
Hazardous Material Identification:
- TSCA:No
- Risk Phrases:R36/37/38
- Storage Condition:0-10°C
Pentafluorophenyltriethoxysilane Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | S12859-5g |
Pentafluorophenyltriethoxysilane |
20083-34-5 | 97% | 5g |
£40.00 | 2022-02-28 | |
| Fluorochem | S12859-25g |
Pentafluorophenyltriethoxysilane |
20083-34-5 | 97% | 25g |
£200.00 | 2022-02-28 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | T162306-1G |
Pentafluorophenyltriethoxysilane |
20083-34-5 | >95.0%(GC) | 1g |
¥354.90 | 2023-08-31 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | T162306-5G |
Pentafluorophenyltriethoxysilane |
20083-34-5 | >95.0%(GC) | 5g |
¥1283.90 | 2023-08-31 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X65295-1g |
Triethoxy(pentafluorophenyl)silane |
20083-34-5 | >95.0%(GC) | 1g |
¥378.0 | 2023-09-05 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X65295-5g |
Triethoxy(pentafluorophenyl)silane |
20083-34-5 | >95.0%(GC) | 5g |
¥1358.0 | 2023-09-05 | |
| BAI LING WEI Technology Co., Ltd. | PC10076-1g |
(Triethoxysilyl)pentafluorobenzene |
20083-34-5 | 1g |
¥ 1320 | 2022-04-26 | ||
| BAI LING WEI Technology Co., Ltd. | PC10076-5g |
(Triethoxysilyl)pentafluorobenzene |
20083-34-5 | 5g |
¥ 2266 | 2022-04-26 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | T3134-5g |
Pentafluorophenyltriethoxysilane |
20083-34-5 | 95.0%(GC) | 5g |
¥2180.0 | 2022-06-09 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | T3134-1g |
Pentafluorophenyltriethoxysilane |
20083-34-5 | 95.0%(GC) | 1g |
¥695.0 | 2022-06-09 |
Pentafluorophenyltriethoxysilane Suppliers
Pentafluorophenyltriethoxysilane Related Literature
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Kohei Ohshiro,Yui Sasaki,Qi Zhou,Xiaojun Lyu,Yusuke Yamanashi,Katsumasa Nakahara,Hirokazu Nagaoka,Tsuyoshi Minami Analyst 2022 147 1055
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Dong-Yeop Yoo,Jiyoon Jung,Young Sang Park,Gwan Hyun Choi,Ho Gyu Yoon,Seung Sang Hwang,Albert S. Lee J. Mater. Chem. A 2023 11 18426
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Jianwen Liu,Sicong He,Shaoqing Liu,Shiquan Wang,Jiujun Zhang J. Mater. Chem. A 2022 10 22929
Additional information on Pentafluorophenyltriethoxysilane
Pentafluorophenyltriethoxysilane (CAS No. 20083-34-5): An Overview of a Versatile Silane Coupling Agent
Pentafluorophenyltriethoxysilane (CAS No. 20083-34-5) is a highly versatile silane coupling agent that has gained significant attention in recent years due to its unique chemical properties and wide range of applications. This compound, often referred to as PFPTES, is characterized by its pentafluorophenyl group and triethoxysilane functionality, which endow it with exceptional reactivity and stability.
The chemical structure of Pentafluorophenyltriethoxysilane consists of a pentafluorophenyl group attached to a silicon atom, which is further bonded to three ethoxy groups. This structure allows the compound to act as a bridge between organic and inorganic materials, making it an ideal choice for various surface modification and material science applications.
One of the key applications of Pentafluorophenyltriethoxysilane is in the field of surface chemistry and material science. It is widely used to modify the surface properties of materials such as glass, silica, and other inorganic substrates. The triethoxysilane group readily reacts with hydroxyl groups on the surface of these materials, forming a stable siloxane bond. This process significantly enhances the adhesion between organic coatings and inorganic substrates, leading to improved mechanical properties and durability.
In addition to its use in surface modification, Pentafluorophenyltriethoxysilane has found applications in the synthesis of advanced materials. Recent research has shown that this compound can be used to functionalize graphene and other two-dimensional materials, enhancing their chemical stability and reactivity. For example, a study published in the Journal of Materials Chemistry A demonstrated that the use of PFPTES for graphene functionalization resulted in improved dispersion and enhanced electrical conductivity.
The pentafluorophenyl group in Pentafluorophenyltriethoxysilane also makes it an excellent reagent for click chemistry reactions. The high electron-withdrawing nature of the fluorine atoms imparts unique reactivity to this group, allowing it to participate in various coupling reactions with high efficiency. This property has been exploited in the development of new pharmaceuticals and biocompatible materials. A recent study published in Organic Letters reported the use of PFPTES in the synthesis of novel drug delivery systems, where it was used to attach targeting ligands to nanoparticles, improving their specificity and efficacy.
Beyond its applications in material science and pharmaceuticals, Pentafluorophenyltriethoxysilane has also been explored for its potential in environmental remediation. The compound's ability to form stable bonds with metal oxides makes it useful for removing heavy metals from contaminated water sources. Research published in Environmental Science & Technology highlighted the effectiveness of PFPTES-modified sorbents in removing lead and cadmium ions from aqueous solutions with high efficiency.
The synthesis of Pentafluorophenyltriethoxysilane typically involves the reaction of pentafluorophenol with triethoxychlorosilane or triethoxy(methyl)silane under controlled conditions. The process requires careful control of temperature and reaction time to ensure high yield and purity. Recent advancements in synthetic methods have led to more efficient and environmentally friendly routes for producing this compound, making it more accessible for large-scale applications.
In conclusion, Pentafluorophenyltriethoxysilane (CAS No. 20083-34-5) is a highly versatile silane coupling agent with a wide range of applications in surface chemistry, material science, pharmaceuticals, and environmental remediation. Its unique chemical structure and properties make it an invaluable tool for researchers and industry professionals seeking to enhance the performance and functionality of various materials and systems. As research continues to uncover new uses for this compound, its importance is likely to grow even further.
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