17648-05-4 Usage
Description
2,5-dimethyl-2,5-diphenyl-hexane, also known as neohexane, is a colorless, crystalline solid with the chemical formula C20H28. It is insoluble in water and is primarily used as a high-quality solvent in various industries.
Uses
Used in Chemical Industry:
2,5-dimethyl-2,5-diphenyl-hexane is used as a solvent for the production of various products such as rubber, adhesives, and coatings. Its high-quality solvent properties make it suitable for these applications.
Used in Pharmaceutical Industry:
2,5-dimethyl-2,5-diphenyl-hexane is used as a solvent in the manufacture of pharmaceuticals. Its ability to dissolve a wide range of substances makes it useful in the production of various medications.
Used in Dye Industry:
2,5-dimethyl-2,5-diphenyl-hexane is used as a solvent in the production of dyes. Its solubility properties allow for the efficient creation of various colored compounds.
Used in Insecticide Industry:
2,5-dimethyl-2,5-diphenyl-hexane is used as a solvent in the manufacture of insecticides. Its ability to dissolve active ingredients makes it a valuable component in the production of these products.
Check Digit Verification of cas no
The CAS Registry Mumber 17648-05-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,4 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17648-05:
(7*1)+(6*7)+(5*6)+(4*4)+(3*8)+(2*0)+(1*5)=124
124 % 10 = 4
So 17648-05-4 is a valid CAS Registry Number.
17648-05-4Relevant articles and documents
Palladium-catalyzed R(sp3)-Zn/R(sp)-SnBu3 oxidative cross-coupling
Jin, Liqun,Zhao, Yingsheng,Wang, Haibo,Lei, Aiwen
, p. 649 - 654 (2008/12/21)
A novel bond formation through oxidative cross-coupling with desyl chloride as the oxidant has been investigated. The coupling can be carried out under mild conditions. The Csp3-center carbon was involved even in the presence of a β-H, and up to 90% of the desired cross-coupling product was obtained with the secondary Csp3-center substrate. Georg Thieme Verlag Stuttgart.
Palladium-catalyzed homocoupling reactions between two Csp3-Csp3 centers
Lei, Aiwen,Zhang, Xumu
, p. 2285 - 2288 (2007/10/03)
(Matrix Presented) A novel palladium-catalyzed coupling reaction between two Csp3-Csp3 centers has been investigated. This protocol is initiated by the oxidative addition of an α-halo carbonyl compound to a palladium(0) species, followed by the double transmetalation. The key dialkyl palladium intermediate undergoes reductive elimination to form the desired coupling product.
