Cas no 238403-28-6 (Ethane-1,2-diol;triphenylphosphane)
Ethane-1,2-diol;triphenylphosphane Chemical and Physical Properties
Names and Identifiers
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- POLY(ETHYLENE GLYCOL) TRIPHENYLPHOSPHINE
- Ethane-1,2-diol;triphenylphosphane
- 238403-28-6
-
- MDL: MFCD03100952
- Inchi: 1S/C18H15P.C2H6O2/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;3-1-2-4/h1-15H;3-4H,1-2H2
- InChI Key: QSHRKZHIILSUDY-UHFFFAOYSA-N
- SMILES: P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.OCCO
Computed Properties
- Exact Mass: 324.12791691g/mol
- Monoisotopic Mass: 324.12791691g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 23
- Rotatable Bond Count: 4
- Complexity: 208
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 40.5
Experimental Properties
- Melting Point: 44-46?°C (lit.)
Ethane-1,2-diol;triphenylphosphane Security Information
- Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:3
Ethane-1,2-diol;triphenylphosphane Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 532649-1G |
Ethane-1,2-diol;triphenylphosphane |
238403-28-6 | 1G |
¥431.57 | 2022-02-24 |
Ethane-1,2-diol;triphenylphosphane Related Literature
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Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
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Amandine Altmayer-Henzien,Valérie Declerck,David J. Aitken,Ewen Lescop,Denis Merlet,Jonathan Farjon Org. Biomol. Chem., 2013,11, 7611-7615
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Yong Ping Huang,Tao Tao,Zheng Chen,Wei Han,Ying Wu,Chunjiang Kuang,Shaoxiong Zhou,Ying Chen J. Mater. Chem. A, 2014,2, 18831-18837
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Tengfei Yu,Yuehan Wu,Wei Li,Bin Li RSC Adv., 2014,4, 34134-34143
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Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
Additional information on Ethane-1,2-diol;triphenylphosphane
Comprehensive Overview of Ethane-1,2-diol and Triphenylphosphane (CAS No. 238403-28-6)
Ethane-1,2-diol, also known as ethylene glycol, is a versatile organic compound with the chemical formula C2H6O2. It is a colorless, odorless, and sweet-tasting liquid that is widely used in various industrial and commercial applications. On the other hand, triphenylphosphane, with the chemical formula C18H15P, is a common organophosphorus compound that plays a crucial role in organic synthesis and catalysis. The combination of these two compounds, as identified by the CAS number 238403-28-6, represents a unique and valuable entity in the field of chemistry and pharmaceuticals.
Ethane-1,2-diol is primarily used as an antifreeze and coolant in automotive and industrial applications due to its excellent heat transfer properties and low freezing point. It is also a key component in the production of polyester fibers, resins, and solvents. In the pharmaceutical industry, ethylene glycol derivatives are used as intermediates in the synthesis of various drugs and active pharmaceutical ingredients (APIs). Recent research has explored the potential of ethylene glycol-based polymers in drug delivery systems, particularly for controlled release applications.
Triphenylphosphane, on the other hand, is a well-known ligand in coordination chemistry and catalysis. It is widely used in palladium-catalyzed cross-coupling reactions, such as the Suzuki-Miyaura coupling and Heck reactions, which are fundamental processes in organic synthesis. The phosphorus atom in triphenylphosphane can form stable complexes with transition metals, making it an essential reagent in the development of new catalysts for various chemical transformations. Recent studies have also highlighted its role in asymmetric synthesis and chiral catalysis, contributing to the advancement of enantioselective reactions.
The combination of Ethane-1,2-diol and Triphenylphosphane (CAS No. 238403-28-6) opens up new possibilities in both synthetic chemistry and pharmaceutical research. One notable application is in the synthesis of complex organic molecules with specific functional groups. For instance, ethylene glycol can serve as a building block for creating multifunctional ligands that can be further modified using triphenylphosphane as a catalyst or ligand. This synergy can lead to the development of novel materials with enhanced properties for use in drug delivery systems, polymer science, and advanced materials.
In the context of pharmaceutical research, the combination of these two compounds has been explored for their potential in improving drug solubility and bioavailability. Ethylene glycol derivatives can enhance the solubility of poorly soluble drugs, while triphenylphosphane can facilitate their chemical modification to achieve desired pharmacological properties. Recent studies have shown that these compounds can be used to create prodrugs that are more stable and have improved pharmacokinetic profiles.
Beyond their individual applications, the interaction between Ethane-1,2-diol and Triphenylphosphane has been studied for their potential in environmental remediation. Ethylene glycol can be used to stabilize metal nanoparticles, which are then functionalized with triphenylphosphane to create highly efficient catalysts for degrading pollutants. This approach has shown promise in treating contaminated water sources and industrial effluents.
In summary, the combination of Ethane-1,2-diol (ethylene glycol) and Triphenylphosphane (CAS No. 238403-28-6) represents a powerful tool in modern chemistry and pharmaceuticals. Their unique properties and synergistic effects offer numerous opportunities for innovation across various fields, from materials science to drug development. As research continues to advance, it is likely that new applications will emerge, further solidifying their importance in both academic and industrial settings.
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