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Tetramethyl-9,10-diphenylanthracene-2,3,6,7-tetracarboxylate is a complex organic compound characterized by its unique molecular structure. It is composed of an anthracene core, which is a tricyclic aromatic hydrocarbon, with two phenyl rings attached at the 9,10 positions. The molecule is further distinguished by the presence of four carboxyl groups (-COOH) at the 2, 3, 6, and 7 positions, and four methyl groups (-CH3) at the anthracene core. tetramethyl-9,10-diphenylanthracene-2,3,6,7-tetracarboxylate is known for its potential applications in various fields, such as organic synthesis, materials science, and as a precursor in the production of certain dyes and pigments. Its chemical properties and reactivity are influenced by the presence of the carboxyl and methyl groups, which can participate in various chemical reactions, such as esterification and substitution. The compound's structure also contributes to its stability and solubility in organic solvents, making it a valuable component in the synthesis of more complex molecules.

811-16-5

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811-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 811-16-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,1 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 811-16:
(5*8)+(4*1)+(3*1)+(2*1)+(1*6)=55
55 % 10 = 5
So 811-16-5 is a valid CAS Registry Number.

811-16-5Relevant academic research and scientific papers

ECHANGE DE SUBSTITUANTS EN SERIE ANTHRACENIQUE PAR CYCLO-ADDITIONS SUIVIES D'ELIMINATIONS SPONTANEES; APPLICATION A LA SYNTHESE D'UN CAPTEUR HYDROSOLUBLE D'OXYGENE SINGULET

Aubry, J. M.,Schmitz, C.,Rigaudy, J.,Cuong, Nguyen Kim

, p. 623 - 628 (2007/10/02)

Condensation of benzaldehyde with veratrole in acidic media affords a one-pot synthesis of 2,3,6,7-tetramethoxy-9,10-diphenylanthracene 1f.The reaction of 1f with dimethyl acetylenedicarboxylate does not yield the expected adduct but leads directly to the tetramethyl 9,10-diphenylanthracene-2,3,6,7-tetracarboxylate 9b and other products, through successive cyclo-additions followed by spontaneous eliminations of dimethoxyacetylene or methoxycarbyne.

A NEW ACCESS TO THE ANTHRACENE CORE. SYNTHESIS OF TWO WATER SOLUBLE SINGLET OXYGEN TRAPS DERIVED FROM 1,3-DIPHENYLISOBENZOFURAN AND 9,10-DIPHENYLANTHRACENE

Schmitz, C.,Aubry, J. M.,Rigaudy, J.

, p. 1425 - 1430 (2007/10/02)

Two water soluble 1O2 traps: dipotassium 1,3-diphenylisobenzofuran-5,6-dicarboxylate and tetrapotassium 9,10-diphenylanthracene-2,3,6,7-tetracarboxylate have been prepared in good yields and a new access to the anthracene skeleton is described.The key-step of this synthesis consists of a cycloaddition between 1,3-diphenylisobenzofurans and dimethyl 7-oxabicyclo-5-heptene-2,3-dicarboxylate; the adducts thus obtained undergo dehydration to afford the corresponding anthracenes.

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