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2-(4-methoxyphenyl)-1,5-diphenyl-1H-pyrrole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1430102-67-2

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1430102-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1430102-67-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,0,1,0 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1430102-67:
(9*1)+(8*4)+(7*3)+(6*0)+(5*1)+(4*0)+(3*2)+(2*6)+(1*7)=92
92 % 10 = 2
So 1430102-67-2 is a valid CAS Registry Number.

1430102-67-2Downstream Products

1430102-67-2Relevant academic research and scientific papers

Synthesis of Polysubstituted Pyrroles via Silver-Catalyzed Oxidative Radical Addition of Cyclopropanols to Imines

Zhou, Yulu,Wu, Mingchang,Liu, Yi,Cheng, Cungui,Zhu, Gangguo

, p. 7542 - 7546 (2020)

A silver-catalyzed formal [3 + 2] cycloaddition reaction, with cyclopropanols as a C3 subunit and imines as a two-atom subunit, is developed. The reaction takes place under mild conditions and produces a broad array of polysubstituted pyrroles in medium t

Preparation method of polysubstituted pyrrole compound

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Paragraph 0025-0029; 0030-0033, (2019/07/04)

The invention discloses a preparation method of a polysubstituted pyrrole compound. The preparation method comprises the following steps: mixing imine shown as a formula II, cyclopropanol shown as a formula III, a catalyst, an oxidant and a solvent to for

Copper-catalyzed decarboxylative coupling of alkynyl carboxylates with 1,1-dibromo-1-alkenes

Huang, Zheng,Shang, Rui,Zhang, Zi-Rong,Tan, Xiao-Dan,Xiao, Xiao,Fu, Yao

, p. 4551 - 4557 (2013/06/05)

A copper-catalyzed decarboxylative coupling reaction of potassium alkynyl carboxylates with 1,1-dibromo-1-alkenes was developed for the synthesis of unsymmetrical 1,3-diyne and 1,3,5-triyne derivatives. Diverse aryl, alkenyl, alkynyl, and alkyl substituted 1,1-dibromo-1-alkenes can react smoothly with aryl and alkyl substituted propiolates to produce unsymmetrical 1,3-diynes and 1,3,5-triynes with high selectivity and good functional group compatibility.

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