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5,10,15-tris(4-carbomethoxyphenyl)tetrapyrrane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

292164-64-8

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292164-64-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 292164-64-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,2,1,6 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 292164-64:
(8*2)+(7*9)+(6*2)+(5*1)+(4*6)+(3*4)+(2*6)+(1*4)=148
148 % 10 = 8
So 292164-64-8 is a valid CAS Registry Number.

292164-64-8Downstream Products

292164-64-8Relevant academic research and scientific papers

Efficient synthesis of 5,10,15-triarylcorroles using Amberlyst 15 under solvent-free conditions

Kumari, Pratibha,Chauhan, Shive M. S.

, p. 779 - 783 (2008)

(Chemical Equation Presented) An efficient and convenient synthesis of 5,10,15-triarylcorroles by the condensation of aryl aldehydes with pyrrole catalyzed by Amberlyst 15 followed by oxidative cyclization with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (D

CORROLE-BASED FRAMEWORKS AND METHODS OF USE THEREOF

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Paragraph 0039; 00171, (2021/02/26)

Described herein are corrole-based frameworks and methods for making the same. The corrole-based frameworks have unique structural and physical properties, which lends them to be versatile in a number of different applications and uses such as in gas stor

Efficient synthesis of meso-substituted corroles in a H2O-MeOH mixture

Koszarna, Beata,Gryko, Daniel T.

, p. 3707 - 3717 (2007/10/03)

New and efficient conditions for the synthesis of meso-substituted corroles were developed. The first step, involving the reaction of aldehydes with pyrrole, was carried out in a water-methanol mixture in the presence of HCl. A relatively narrow distribut

Optimizing the synthesis of 5,10-disubstituted tripyrromethanes

Ka, Jae-Won,Lee, Chang-Hee

, p. 4609 - 4613 (2007/10/03)

Condensation of aldehydes with pyrrole in the presence of acid catalyst gave the mixture of dipyrromethanes and tripyrromethanes. The major product was switched from dipyrromethanes to tripyrromethanes according to the sequence of adding the reactants and

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