Cas no 21692-54-6 (2-(Cyclohexen-1-yl)ethynyl-triethyl-silane)
2-(Cyclohexen-1-yl)ethynyl-triethyl-silane Chemical and Physical Properties
Names and Identifiers
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- 2-(cyclohexen-1-yl)ethynyl-triethyl-silane
- 2-(Cyclohexen-1-yl)ethynyl-triethylsilane
- D96877
- 21692-54-6
- MFCD33022300
- (Cyclohex-1-en-1-ylethynyl)triethylsilane
- PS-18535
- [2-(cyclohex-1-en-1-yl)ethynyl]triethylsilane
- Cyclohexene, 1-[2-(triethylsilyl)ethynyl]-
- SY323165
- 2-(Cyclohexen-1-yl)ethynyl-triethyl-silane
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- MDL: MFCD33022300
- Inchi: 1S/C14H24Si/c1-4-15(5-2,6-3)13-12-14-10-8-7-9-11-14/h10H,4-9,11H2,1-3H3
- InChI Key: KBTOOJLYPFWADT-UHFFFAOYSA-N
- SMILES: [Si](C#CC1=C([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H])(C([H])([H])C([H])([H])[H])(C([H])([H])C([H])([H])[H])C([H])([H])C([H])([H])[H]
Computed Properties
- Exact Mass: 220.164727300g/mol
- Monoisotopic Mass: 220.164727300g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 15
- Rotatable Bond Count: 5
- Complexity: 275
- 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: 0
2-(Cyclohexen-1-yl)ethynyl-triethyl-silane Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| eNovation Chemicals LLC | Y1009955-1G |
2-(cyclohexen-1-yl)ethynyl-triethyl-silane |
21692-54-6 | 97% | 1g |
$170 | 2024-07-21 | |
| eNovation Chemicals LLC | Y1009955-5G |
2-(cyclohexen-1-yl)ethynyl-triethyl-silane |
21692-54-6 | 97% | 5g |
$485 | 2024-07-21 | |
| eNovation Chemicals LLC | Y1009955-10G |
2-(cyclohexen-1-yl)ethynyl-triethyl-silane |
21692-54-6 | 97% | 10g |
$810 | 2024-07-21 | |
| eNovation Chemicals LLC | Y1009955-25G |
2-(cyclohexen-1-yl)ethynyl-triethyl-silane |
21692-54-6 | 97% | 25g |
$1785 | 2024-07-21 | |
| Aaron | AR01KYQY-100mg |
2-(cyclohexen-1-yl)ethynyl-triethyl-silane |
21692-54-6 | 97% | 100mg |
$44.00 | 2025-02-12 | |
| Aaron | AR01KYQY-250mg |
2-(cyclohexen-1-yl)ethynyl-triethyl-silane |
21692-54-6 | 97% | 250mg |
$59.00 | 2025-02-12 | |
| Aaron | AR01KYQY-10g |
2-(cyclohexen-1-yl)ethynyl-triethyl-silane |
21692-54-6 | 97% | 10g |
$734.00 | 2025-02-12 | |
| Aaron | AR01KYQY-25g |
2-(cyclohexen-1-yl)ethynyl-triethyl-silane |
21692-54-6 | 97% | 25g |
$1614.00 | 2025-02-12 | |
| Aaron | AR01KYQY-100g |
2-(cyclohexen-1-yl)ethynyl-triethyl-silane |
21692-54-6 | 97% | 100g |
$4070.00 | 2023-12-14 | |
| 1PlusChem | 1P01KYIM-100mg |
2-(cyclohexen-1-yl)ethynyl-triethyl-silane |
21692-54-6 | 97.00% | 100mg |
$38.00 | 2023-12-19 |
2-(Cyclohexen-1-yl)ethynyl-triethyl-silane Suppliers
2-(Cyclohexen-1-yl)ethynyl-triethyl-silane Related Literature
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Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860
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Jacob S. Jordan,Evan R. Williams Analyst, 2021,146, 2617-2625
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Marcin Czapla,Jack Simons Phys. Chem. Chem. Phys., 2018,20, 21739-21745
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Partha Laskar,Christine Dufès Nanoscale Adv., 2021,3, 6007-6026
Additional information on 2-(Cyclohexen-1-yl)ethynyl-triethyl-silane
2-(Cyclohexen-1-yl)ethynyl-triethyl-silane: A Comprehensive Overview
The compound with CAS No. 21692-54-6, commonly referred to as 2-(Cyclohexen-1-yl)ethynyl-triethyl-silane, is a fascinating molecule that has garnered significant attention in the fields of organic chemistry and materials science. This compound is a derivative of triethylsilane, a well-known organosilicon compound, and features a unique structure that combines a cyclohexene ring with an ethynyl group. The combination of these functional groups imparts distinctive chemical properties, making it a valuable tool in various research and industrial applications.
2-(Cyclohexen-1-yl)ethynyl-triethyl-silane is synthesized through a series of well-established organic reactions. The synthesis typically involves the coupling of cyclohexene with an appropriate ethynylating agent in the presence of triethylsilane. This reaction pathway is not only efficient but also highlights the versatility of organosilicon compounds in facilitating complex molecular transformations. Recent studies have explored alternative synthetic routes, leveraging transition metal catalysts to enhance reaction efficiency and yield.
One of the most notable applications of 2-(Cyclohexen-1-yl)ethynyl-triethyl-silane is in the field of polymer chemistry. The compound serves as a precursor for the synthesis of advanced polymers with tailored mechanical and thermal properties. Researchers have demonstrated that incorporating this compound into polymer networks can significantly improve their tensile strength and thermal stability. These findings have opened new avenues for its use in high-performance materials, such as those required in aerospace and automotive industries.
In addition to its role in polymer synthesis, 2-(Cyclohexen-1-yl)ethynyl-triethyl-silane has also found applications in organic electronics. The compound's ability to act as a versatile building block for constructing conjugated systems has been exploited in the development of novel semiconducting materials. Recent breakthroughs in this area have leveraged its unique electronic properties to design more efficient organic photovoltaic devices, which are critical for advancing renewable energy technologies.
The cyclohexene moiety in 2-(Cyclohexen-1-yl)ethynyl-triethyl-silane contributes significantly to its reactivity and stability. Studies have shown that the conjugation between the cyclohexene ring and the ethynyl group enhances the molecule's ability to participate in various chemical transformations, such as cross-coupling reactions and cycloadditions. These reactions are pivotal in synthesizing complex organic molecules with potential applications in pharmaceuticals and agrochemicals.
Recent advancements in computational chemistry have provided deeper insights into the electronic structure and reactivity of 2-(Cyclohexen-1-yl)ethynyl-triethyl-silane. High-level quantum mechanical calculations have revealed that the molecule exhibits unique frontier molecular orbitals, which are responsible for its exceptional reactivity under specific conditions. This understanding has enabled chemists to design more efficient reaction protocols, further expanding its utility in synthetic chemistry.
In conclusion, 2-(Cyclohexen-1-yl)ethynyl-triethyl-silane (CAS No. 21692-54-6) stands out as a versatile and valuable compound with diverse applications across multiple disciplines. Its unique structure, combined with recent advancements in synthetic and computational methodologies, positions it as a key player in driving innovation in materials science, organic electronics, and polymer chemistry. As research continues to uncover new facets of its properties and potential uses, this compound is poised to make even greater contributions to scientific progress.
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