6880-74-6 Usage
Uses
Used in Organic Synthesis:
Trinaphthylene-5,6,11,12,17,18-hexone is used as a key intermediate in the synthesis of various organic compounds due to its reactive properties and unique structure. Its presence in the synthesis process can lead to the formation of new compounds with potential applications in different industries.
Used in Materials Chemistry:
Trinaphthylene-5,6,11,12,17,18-hexone is used as a building block in the development of new materials with enhanced properties. Its high thermal stability and rigid structure make it an ideal candidate for creating materials with improved performance in high-temperature environments.
Used in Pharmaceutical Applications:
Trinaphthylene-5,6,11,12,17,18-hexone is used as a starting material or a component in the synthesis of pharmaceutical compounds. Its unique structure and reactivity can contribute to the development of new drugs with potential therapeutic applications.
Used in Electronics:
Trinaphthylene-5,6,11,12,17,18-hexone is used in the development of electronic materials, such as organic semiconductors and conductive polymers, due to its aromatic nature and potential for molecular interactions. This can lead to the creation of new electronic devices with improved performance and efficiency.
Used in Advanced Materials:
Trinaphthylene-5,6,11,12,17,18-hexone is used as a component in the creation of advanced materials with unique properties, such as high thermal stability, rigidity, and potential for molecular interactions. These materials can be used in various applications, including aerospace, automotive, and construction industries.
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 academic research and scientific papers
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.
Dimeric Naphthoquinones, XIV. - Intermediates of the cyclo-Trimerization of Naphthoquinone: Synthesis of Hydroxyheptastarphenequinones
Laatsch, Hartmut
, p. 605 - 619 (2007/10/02)
Dehydrogenation of heptastarphene-5,6,11,12,17,18-hexaol (3a) with one molar equivalent of 1,4-naphthoquinone (1) yields nearly quantitatively the blue-green 5,12,17,18-tetrahydroxyheptastarphene-6,11-quinone 4.Oxidation of 3a with two molar equivalents of 1 affords a 4/6 mixture of the expected diquinone 5.From the yellow tetraacetate 7b were obtained by regioselective deacetylation the blue triacetate 7c, the blue-green diacetate 9, its isomer 11 and, by rearrangement, red 14a.Oxidation of 7c yields 8a, the acetate of the intermediate 5 of the 3a dehydrogenation. 9 and 11 are oxidized by silver oxide to give the green diquinone 10a and the violet 12a, respectively, which both rearrange in pyridine by acyl migration forming 8a.The colour of the quinones is due to donor-acceptor interactions.
