6006-33-3 Usage
Uses
Used in the Chemical Industry:
N-Tridecylcyclohexane is used as a solvent for its ability to dissolve nonpolar substances, which is crucial in various chemical processes and reactions.
Used in the Plastics Industry:
It serves as an ingredient in the production of plastics, contributing to the manufacturing process due to its compatibility with polymers and its ability to improve product properties.
Used in the Cosmetics Industry:
N-Tridecylcyclohexane is used as an ingredient in cosmetics for its ability to enhance the spreadability and gloss of personal care products, improving their texture and appearance.
Used in the Coatings Industry:
It is utilized in the formulation of coatings to improve their spreadability and gloss, ensuring a high-quality finish in applications such as paints and varnishes.
Check Digit Verification of cas no
The CAS Registry Mumber 6006-33-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,0 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6006-33:
(6*6)+(5*0)+(4*0)+(3*6)+(2*3)+(1*3)=63
63 % 10 = 3
So 6006-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C19H38/c1-2-3-4-5-6-7-8-9-10-11-13-16-19-17-14-12-15-18-19/h19H,2-18H2,1H3
6006-33-3Relevant academic research and scientific papers
Total syntheses of all tri-oxygenated 16-phytoprostane classes: Via a common precursor constructed by oxidative cyclization and alkyl-alkyl coupling reactions as the key steps
Smr?ek, Jakub,Pohl, Radek,Jahn, Ullrich
supporting information, p. 9408 - 9414 (2017/11/22)
A unified strategy for the total synthesis of the methyl esters of all phytoprostane (PhytoP) classes bearing two ring-oxygen atoms based on an orthogonally protected common precursor is described. Racemic 16-F1t-, 16-E1-PhytoP and their C-16 epimers, which also occur as racemates in Nature, were successfully obtained. The first total synthesis of very sensitive 16-D1t-PhytoP succeeded, however, it quickly isomerized to more stable, but so far also unknown Δ13-16-D1t-PhytoP, which may serve as a more reliable biomarker for D-type PhytoP. The dioxygenated cyclopentane ring carrying the ω-chain with the oxygen functionality in the 16-position was approached by a radical oxidative cyclization mediated by ferrocenium hexafluorophosphate and TEMPO. The α-chain was introduced by a new copper-catalyzed alkyl-alkyl coupling of a 6-heptenyl Grignard reagent with a functionalized cyclopentylmethyl triflate.
