66003-79-0 Usage
Uses
Used in Chemical Synthesis:
2,6-dicyclopentylphenol is used as a chemical intermediate for the synthesis of various compounds in the chemical industry. Its unique structure allows it to be a key component in the production of specialty chemicals and materials.
Used in Material Science:
In the field of material science, 2,6-dicyclopentylphenol is used as a building block for the development of new materials with specific properties. Its incorporation into polymers or other materials can enhance their characteristics, such as thermal stability or chemical resistance.
Used in Pharmaceutical Industry:
2,6-dicyclopentylphenol is used as a starting material or a component in the synthesis of pharmaceutical compounds. Its unique chemical structure can contribute to the development of new drugs with potential therapeutic applications.
Used in Research and Development:
2,6-dicyclopentylphenol is utilized in research and development settings to explore its potential applications and properties. Scientists and researchers use 2,6-dicyclopentylphenol to investigate its reactivity, stability, and interactions with other chemicals, which can lead to the discovery of new applications and uses.
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.
