10143-60-9 Usage
Description
DI(2-ETHYLHEXYL) ETHER, also known as Ethylhexyl Oxide, is a chemical compound derived from the ethylhexyl group. It is an organic ether with the molecular formula C16H34O. DI(2-ETHYLHEXYL) ETHER is characterized by its high efficiency as a catalyst and its ability to form derivatives with other materials.
Uses
Used in Chemical Catalysts:
DI(2-ETHYLHEXYL) ETHER is used as a catalyst in the chemical industry for its high efficiency in promoting various chemical reactions. Its derivative over Nafion-H, a perfluoroalkanesulfonic acid, is particularly effective as a solid catalyst, enhancing the rate of reactions and improving overall process efficiency.
Used in Polymer Science:
In the field of polymer science, DI(2-ETHYLHEXYL) ETHER can be used as a component in the synthesis of various polymers due to its reactive ethylhexyl groups. This application can lead to the development of new materials with specific properties tailored for different industries.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, DI(2-ETHYLHEXYL) ETHER could potentially be used in the pharmaceutical industry as a solvent or intermediate in the synthesis of drugs, given its chemical properties and reactivity.
Used in Environmental Applications:
The high efficiency of DI(2-ETHYLHEXYL) ETHER as a catalyst may also find applications in environmental science, particularly in processes that require the conversion or breakdown of pollutants. Its use in this context could contribute to the development of more sustainable and eco-friendly technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 10143-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,4 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10143-60:
(7*1)+(6*0)+(5*1)+(4*4)+(3*3)+(2*6)+(1*0)=49
49 % 10 = 9
So 10143-60-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H34O/c1-5-9-11-15(7-3)13-17-14-16(8-4)12-10-6-2/h15-16H,5-14H2,1-4H3
10143-60-9Relevant articles and documents
Silver(I)-Catalyzed Reductive Cross-Coupling of Aldehydes to Structurally Diverse Cyclic and Acyclic Ethers
Dong, Guichao,Li, Chuang,Liang, Ting,Xu, Xin,Xu, Zhou
supporting information, p. 1817 - 1821 (2022/03/16)
A range of medium-sized cyclic ethers (5 to 11 membered) have been effectively synthesized through intramolecular reductive coupling of dialdehydes initiated by 50 ppm to 0.5% of AgNTf2 with hydrosilane at 25 °C. The catalytic system is also suitable for the coupling of two different monoaldehydes to provide unsymmetrical ethers. This protocol features broad functional group compatibility, high product diversity, high efficiency, and utility in the late-stage modification of complex biorelevant molecules.
SATURATED HOMOETHER MANUFACTURING METHOD FROM UNSATURATED CARBONYL COMPOUND
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Paragraph 0039; 0044, (2020/05/14)
PROBLEM TO BE SOLVED: To provide a method for manufacturing saturated homoether from an unsaturated carboxyl compound at good efficiency. SOLUTION: There is provided a manufacturing method of saturated homoether using an unsaturated carboxyl compound and hydrogen as raw materials, and a catalyst in which a metal is carried on an acidic catalyst carrier. The metal of the catalyst is for example palladium, and the carrier of the catalyst is alumina, silica, silica-alumina, or the like. The unsaturated carbonyl compound as the raw material is 2-butenal, 2-ethyl-2-hexenal, 2-ethyl-2-butenal, 2-hexenal, and manufactured saturated homoether is dibuthylether, bis(2-ethylhexyl)ether, bis(2-ethylbuty)ether, dihexylether, or the like. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPO&INPIT
