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1H-Pyrrole-3,4-dicarboxylic acid, 1-(4-chlorophenyl)-2,5-diphenyl, diethyl ester is a complex organic compound with the molecular formula C25H21ClN2O4. It is a derivative of 1H-pyrrole-3,4-dicarboxylic acid, featuring a 4-chlorophenyl group at the 1-position and two phenyl groups at the 2 and 5 positions. The diethyl ester functional group is present, indicating that the carboxylic acid groups are esterified with ethanol. 1H-Pyrrole-3,4-dicarboxylic acid, 1-(4-chlorophenyl)-2,5-diphenyl-, diethyl ester is characterized by its unique molecular structure, which includes a pyrrole ring, a chlorine atom, and multiple phenyl rings. It is likely to be used in the synthesis of various pharmaceuticals, agrochemicals, or other specialty chemicals due to its diverse functional groups and potential for further chemical reactions.

86397-90-2

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86397-90-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86397-90-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,3,9 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86397-90:
(7*8)+(6*6)+(5*3)+(4*9)+(3*7)+(2*9)+(1*0)=182
182 % 10 = 2
So 86397-90-2 is a valid CAS Registry Number.

86397-90-2Downstream Products

86397-90-2Relevant academic research and scientific papers

Synthesis of highly substituted pyrroles via oxidative free radical reactions of β-aminocinnamates

Tsai, An-I.,Chuang, Che-Ping

, p. 2235 - 2239 (2007/10/03)

Oxidative free radical reactions of β-aminocinnamates are described. Imine radicals produced by tetra-n-butylammonium cerium(IV) nitrate (TBACN) oxidation of enamines undergo efficient addition to the C-C double bond of β-aminocinnamates. This TBACN media

Oxidative free radical reactions of enamino esters

Chuang, Che-Ping,Wu, Yi-Lung

, p. 1841 - 1847 (2007/10/03)

Oxidative free radical reactions of enamino esters are described. Electrophilic carbon-centered radicals produced by the cerium(IV) ammonium nitrate (CAN) oxidation of β-dicarbonyl compounds undergo efficient addition to the C-C double bond of enamino est

Hypervalent iodine in synthesis. 62: A tandem dimerization-cyclocondensation of enamine-esters with [bis(trifluoroacetoxy)iodo]benzene: A method of synthesis of highly substituted pyrroles

Zhang,Chen

, p. 1619 - 1624 (2007/10/03)

A tandem dimerization-cyclocondensation of enamine-esters with [bis(trifluoroacetoxy)iodo]benzene(BTI) provides an effective method for synthesis of highly substituted pyrroles.

OXIDATION OF ENAMINE-ESTERS WITH LEAD TETRA-ACETATE - PART 3. β-AMINOCINNAMATES AND β-AMINOCROTONATES

Sukari, Mohamed A.,Vernon, John M.

, p. 793 - 796 (2007/10/02)

Oxidation of β-aminocinnamates and β-aminocrotonates with lead tetra-acetate gives fully substituted pyrrole-3,4-diesters.

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