66003-79-0 Usage
General Description
2,6-dicyclopentylphenol is a chemical compound that falls under the category of phenols. This organic compound is made up of a phenol which is a single benzene ring bonded to a hydroxy group, and two cyclopentyl groups at the 2nd and 6th positions of the ring. This chemical structure gives it unique properties which are utilized in various industrial applications. The exact toxicity and safety data regarding 2,6-dicyclopentylphenol are limited, hence it needs to be handled with caution. Its physical properties, potential usage, and other specifications should be thoroughly reviewed before handling. As with all chemicals, personal protective equipment should be used to avoid direct skin contact or inhalation.
Check Digit Verification of cas no
The CAS Registry Mumber 66003-79-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,0 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66003-79:
(7*6)+(6*6)+(5*0)+(4*0)+(3*3)+(2*7)+(1*9)=110
110 % 10 = 0
So 66003-79-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H22O/c17-16-14(12-6-1-2-7-12)10-5-11-15(16)13-8-3-4-9-13/h5,10-13,17H,1-4,6-9H2
66003-79-0Relevant articles and documents
Cobalt-Nitrenoid Insertion-Mediated Amidative Carbon Rearrangement via Alkyl-Walking on Arenes
Lee, Jeonghyo,Kang, Bora,Kim, Dongwook,Lee, Jia,Chang, Sukbok
supporting information, p. 18406 - 18412 (2021/11/16)
We herein disclose the Cp*Co(III)(LX)-catalyzed amidative alkyl migration using 2,6-disubstituted phenyl azidoformates. Upon the cobalt-nitrenoid insertion toward the substituted ortho carbon, an arenium cationic species bearing a quaternary carbon is generated, and a subsequent alkyl migration process is suggested to occur through an unforeseen alkyl-walking mechanism. A quinolinol ligand of the cobalt catalyst system is proposed to facilitate the final product-releasing rearomatization process by serving as an internal base. This new mechanistic mode enabled both [1,2]- and [1,4]-alkyl rearrangements to allow the structural variation of N-heterocyclic compounds.
