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2,7-di-tert-butylanthracene-9,10-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18798-85-1

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18798-85-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18798-85-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,9 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18798-85:
(7*1)+(6*8)+(5*7)+(4*9)+(3*8)+(2*8)+(1*5)=171
171 % 10 = 1
So 18798-85-1 is a valid CAS Registry Number.

18798-85-1Downstream Products

18798-85-1Relevant academic research and scientific papers

NOVEL SOLUBLE COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICES

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Page 22, (2010/02/07)

A novel soluble compound which is a distyrylarylene derivative having a soluble substituent and a specific central group and having a solubility of 0.5% by weight or greater at 20°C in an organic solvent; and an organic electroluminescence device having an organic thin film layer which has a single layer or a plurality of layers, is disposed between a cathode and an anode and has at least one layer containing the novel soluble compound. The organic thin film layer can be formed in accordance with a wet process, and the organic electroluminescence device exhibiting a great efficiency of light emission can be produced easily.

SYNTHESIS OF SUBSTITUTED tert-BUTYLANTHRAQUINONES

Pozdnyakovich, Yu. V.,Savyak, R. P.,Shein, S. M.

, p. 532 - 538 (2007/10/02)

The oxidation of 2-methyl-5-tert-butyldiphenylmethane and its 4'-methyl-, chloro-, and nitro-substituded derivatives by potassium permangate in a mixture of pyridine and water leads to the formation of the correspoding 2-benzoyl-4-tert-butyl-benzoic acids, which are converted by the action of sulfuric acid with heat into substituted 2-tert-butylanthraquinones.The cyclization of 2-benzoyl-4-tert-butylbenzoic acids containig a tert-butyl group or chlorine atom in the benzoyl ring is accompanied by a Hayashi rearrangement, which leads to the formation of mixtures thecorresponding 2,6- and 2,7-disubstituted anthraquinones.

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