6880-74-6 Usage
General Description
Trinaphthylene-5,6,11,12,17,18-hexone is a synthetic polycyclic aromatic compound that belongs to the class of naphthalenes. It is a highly stable molecule that is commonly used in organic synthesis and materials chemistry due to its unique structure and reactive properties. This chemical compound is known for its high thermal stability, making it ideal for use in high-temperature applications. Trinaphthylene-5,6,11,12,17,18-hexone is also a versatile building block in the creation of new materials and compounds, with potential applications in fields such as pharmaceuticals, electronics, and advanced materials. Additionally, its aromatic nature and rigid structure make it a valuable tool in the study of molecular interactions and organic reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 6880-74-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,8 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6880-74:
(6*6)+(5*8)+(4*8)+(3*0)+(2*7)+(1*4)=126
126 % 10 = 6
So 6880-74-6 is a valid CAS Registry Number.
6880-74-6Relevant articles and documents
cyclo-Trimerisation of 1,4-Naphthoquinone; Cooperation of Phenol/Quinone Additions and Redox Reactions
Brockmann, Hans
, p. 1 - 8 (2007/10/02)
The reaction course postulated for the cyclo-trimerisation of 1,4-naphthoquinone (1a) to cyclo-tri-1,4-naphthoquinone (11a) is confirmed and supplemented by: (i) isolation of the red intermediate 1',4'-dihydroxy-2,2'-binaphthyl-1,4-quinone (5a), (ii) synthesis of 11a starting from 5a or 2,2'-binaphthyl-1,4:1'4'-diquinone (6a), and (iii) reduction of 5a and 6a by 1,4-naphthalenediol (2a) to 2,2'-binaphthyl-1,1',4,4'-tetrol (4a).Requirement for the cyclo-trimerisation of 1a to 11a is a cooperation of phenol/quinone additions and redox reactions controlled by the permanent decreasing oxidation potential of the reaction mixture.As byproducts of the synthesis of 11a in acetic acid 9a, 10a, 12a, 12c, 13a, 13c, and 14a could be isolated as acetates.
