1665-86-7 Usage
Appearance
Yellow crystalline solid The compound's physical form is a yellow-colored solid with a crystalline structure.
Use as a radical scavenger
Inhibits autoxidation of organic materials 2,6-di-tert-butyl-4-methyl-4-nitrocyclohexa-2,5-dien-1-one is commonly used to prevent the oxidation of organic materials, making it useful in various industrial applications.
Applications in polymer and coating production
Creation of polymers, coatings, and other industrial materials The compound's ability to inhibit autoxidation makes it valuable in the production of various materials, including polymers and coatings.
Use as a reagent in organic synthesis
Formation of carbon-carbon bonds 2,6-di-tert-butyl-4-methyl-4-nitrocyclohexa-2,5-dien-1-one is also used as a reagent in organic synthesis, particularly for forming carbon-carbon bonds.
Reactivity and potential toxicity
Proper safety precautions and handling procedures required Due to the compound's reactivity and potential toxicity, it is essential to follow appropriate safety measures and handling procedures when working with it.
Check Digit Verification of cas no
The CAS Registry Mumber 1665-86-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,6 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1665-86:
(6*1)+(5*6)+(4*6)+(3*5)+(2*8)+(1*6)=97
97 % 10 = 7
So 1665-86-7 is a valid CAS Registry Number.
1665-86-7Relevant articles and documents
THE KINETICS OF THE REACTIONS OF 2,6-DI-t-BUTYL-4-METHYLPHENOL AND 2,4,6-TRIMETHYLPHENOL WITH NITROGEN DIOXIDE IN SOLUTION
Coombes, Robert G.,Diggle, Andrew W.,Kempsell, Stewart P.
, p. 2037 - 2040 (1986)
The reaction of 2,6-di-t-butyl-4-methylphenol with nitrogen dioxide to form 2,6-di-t-butyl-4-methyl-4-nitrocyclohexa-2,5-dienone has a first order dependence of rate on the concentration of the species N2O4.By contrast the observed rate of the correspondi
Iron-Mediated Radical Nitrohalogenation Reactions of Enynes with tert -Butyl Nitrite
Ge, Yaxin,Li, Lijun,Li, Zejiang,Ren, Yingming,Tian, Yunfei,Wu, Jilai,Yan, Qinqin,Yang, Yujie
supporting information, p. 1192 - 1196 (2021/06/28)
A radical nitrohalogenation/cyclization of various enynes with tert -butyl nitrite has been developed that conveniently introduces useful nitro and halo groups into organic compounds. Some control experiments were performed to elucidate the mechanism. Fur
Reactions of 4-Methyl-2,6-diphenylphenol and 4-Nitro-2,6-diphenylphenol with Nitrogen Dioxide
Hartshorn, Michael P.,Martyn, Robert J.,Robinson, Ward T.,Sutton, Kevin H.,Vaughan, John,White, Jonathon M.
, p. 1613 - 1630 (2007/10/02)
Reactions of 4-methyl-2,6-diphenylphenol (11a) with nitrogen dioxide in benzene solution gives the polysubstituted cyclohex-2-enones (14), (15), (16), (17) and (18) via the 4-nitro dienone (13).The reversibility of the 4-nitro dienone (13)/4-hydroxy dieno
