35579-37-4 Usage
General Description
2,6-di(propan-2-yl)cyclohexanone, also known as "dipropylene glycol cyclohexanone," is a chemical compound with the molecular formula C12H22O. It is a colorless liquid with a faint, peppermint-like odor, and is primarily used as a high-boiling solvent in various industrial applications, such as inks, coatings, and adhesives. It is also used as a secondary plasticizer in PVC formulations and as a fragrance ingredient in personal care products. Due to its low volatility and high solvency power, 2,6-di(propan-2-yl)cyclohexanone is valued for its ability to dissolve a wide range of substances, making it versatile for different manufacturing processes. However, it is important to handle this chemical with care, as it may cause skin and eye irritation and is harmful if swallowed.
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 articles and documents
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.
