35579-37-4 Usage
Uses
Used in Inks, Coatings, and Adhesives:
2,6-di(propan-2-yl)cyclohexanone is used as a high-boiling solvent in the manufacturing of inks, coatings, and adhesives. Its ability to dissolve a wide range of substances contributes to the performance and quality of these products.
Used in Plastics Industry:
In the plastics industry, 2,6-di(propan-2-yl)cyclohexanone is used as a secondary plasticizer in PVC formulations. It enhances the flexibility and workability of PVC materials, improving their overall properties.
Used in Personal Care Products:
2,6-di(propan-2-yl)cyclohexanone is used as a fragrance ingredient in personal care products due to its faint, peppermint-like odor. It adds a pleasant scent to products while also providing some solubility benefits for other ingredients.
It is important to handle 2,6-di(propan-2-yl)cyclohexanone with care, as it may cause skin and eye irritation and is harmful if swallowed. Proper safety measures should be taken during its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 35579-37-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,7 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35579-37:
(7*3)+(6*5)+(5*5)+(4*7)+(3*9)+(2*3)+(1*7)=144
144 % 10 = 4
So 35579-37-4 is a valid CAS Registry Number.
35579-37-4Relevant academic research and scientific papers
Magnesium amide base-mediated enantioselective deprotonation processes
Henderson, Kenneth W,Kerr, William J,Moir, Jennifer H
, p. 4573 - 4587 (2007/10/03)
A novel homochiral magnesium bisamide has been readily prepared and, following careful optimisation, this species has been shown to react efficiently with a series of prochiral 4-substituted cyclohexanones in the presence of TMSCl to give the corresponding silyl enol ethers in enantiomeric ratios of up to 95:5. Additionally, the same chiral base system has been shown to be highly effective in the desymmetrisation of cis-2,6-disubstituted cyclohexanones, providing excellent levels of both conversion and enantioselection (up to >99.5:0.5 er). Furthermore, the magnesium bisamide has also been shown to mediate a kinetic resolution process with the corresponding trans-disubstituted substrates, allowing access to enantioenriched enol ethers and ketones.
Enantioselective deprotonation of 2,6-disubstituted cyclohexanones with a homochiral magnesium amide base and the observation of a novel kinetic resolution process
Henderson,Kerr,Moir
, p. 1253 - 1256 (2007/10/03)
A recently developed homochiral magnesium amide base has been shown to be highly effective in the asymmetric deprotonation of cis-2,6-disubstituted cyclohexanones, affording excellent levels of both conversion and enantioselection (up to >99.5:0.5 e.r.).
