4821-19-6 Usage
Description
2.6-Dicyclohexylphenol is an organic compound with the molecular formula C18H26O. It is a white crystalline solid that is characterized by its phenolic structure and two cyclohexyl rings attached to the benzene ring. 2.6-DICYCLOHEXYLPHENOL is known for its antioxidant properties and is used in various applications across different industries.
Uses
Used in Pharmaceutical Industry:
2.6-Dicyclohexylphenol is used as an analogue of the general anesthetic Propofol (P829750) for its sedative and hypnotic effects. It is utilized in the development of anesthetic agents due to its ability to induce a state of unconsciousness and amnesia during medical procedures.
Used in Plastics and Polymer Industry:
2.6-Dicyclohexylphenol is used as an antioxidant in isotactic polypropylene, a thermoplastic polymer. It helps to prevent the oxidative degradation of the polymer, thereby extending its shelf life and improving its overall performance. The antioxidant property of 2.6-Dicyclohexylphenol makes it a valuable additive in the production of plastics and polymers, ensuring their durability and resistance to environmental factors.
Check Digit Verification of cas no
The CAS Registry Mumber 4821-19-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,2 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4821-19:
(6*4)+(5*8)+(4*2)+(3*1)+(2*1)+(1*9)=86
86 % 10 = 6
So 4821-19-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H26O/c19-18-16(14-8-3-1-4-9-14)12-7-13-17(18)15-10-5-2-6-11-15/h7,12-15,19H,1-6,8-11H2
4821-19-6Relevant articles and documents
Titanium salalen catalysts based on cis-1,2-diaminocyclohexane: Enantioselective epoxidation of terminal non-conjugated olefins with H 2O2
Berkessel, Albrecht,Guenther, Thomas,Wang, Qifang,Neudoerfl, Joerg-M.
supporting information, p. 8467 - 8471 (2013/09/02)
Terminal, non-conjugated olefins, such as 1-octene, are difficult to epoxidize asymmetrically. Ti salalen complexes based on cis-1,2- diaminocyclohexane catalyze this demanding reaction giving high yields and enantioselectivities (up to 95 % ee), with H2O2 as the oxidant. The X-ray structures of the μ-oxo and peroxo complexes shed light on the coordination behavior of this novel class of ligands.
ALKYLATION OF HYDROXYARENES WITH OLEFINS, ALCOHOLS AND ETHERS IN IONIC LIQUIDS
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Page/Page column 18-19, (2008/06/13)
Hydroxyarenes are alkylated using an ionic liquid catalyst system with olefins, alcohols, or ethers as alkylating agents. The ionic liquid catalyst system comprises chloroindate (III) anions. The reactions may be conducted at moderate temperatures and pressures to yield commercially relevant alkylated hydroxyarene compounds.
Intramolecular Arene Hydrogenation at Niobium Metal Centres: Stereochemical Consequences
Steffey, Bryan D.,Rothwell, Ian P.
, p. 213 - 215 (2007/10/02)
Selective hydrogenation of 2,6-diphenylphenoxide to 2,6-dicyclohexylphenoxide ligands takes place at niobium(v) metal centres.