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1-(4-bromophenyl)-3,4-diphenyl-1H-pyrrole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102467-65-2

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102467-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102467-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,4,6 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 102467-65:
(8*1)+(7*0)+(6*2)+(5*4)+(4*6)+(3*7)+(2*6)+(1*5)=102
102 % 10 = 2
So 102467-65-2 is a valid CAS Registry Number.

102467-65-2Downstream Products

102467-65-2Relevant academic research and scientific papers

Manganese (III) acetate mediated synthesis of polysubstituted pyrroles under solvent-free ball milling

Zeng, Ji-Chao,Xu, Hui,Yu, Fei,Zhang, Ze

, p. 674 - 678 (2017)

Under solvent-free ball milling conditions, a simple and mild method was developed for efficient synthesis of 2,5-dimethyl-3,4-dicarboxylate-pyrroles and N-substituted 3,4-diphenylpyrroles via condensation-annulation of amines with acetoacetate and 2-phen

The Synergistic Effect between Triphenylpyrrole Isomers as Donors, Linking Groups, and Acceptors on the Fluorescence Properties of D–π–A Compounds in the Solid State

Lei, Yunxiang,Lai, Yueyin,Dong, Lichao,Shang, Guojun,Cai, Zhengxu,Shi, Jianbing,Zhi, Junge,Li, Pengfei,Huang, Xiaobo,Tong, Bin,Dong, Yuping

, p. 434 - 442 (2018)

Eight donor–π–acceptor (D–π–A) compounds employing triphenylpyrrole isomers (TPP-1,2,5 and TPP-1,3,4) as donors, malononitrile (CN) and 1H-indene-1,3(2H)-dione (CO) as acceptors, pyridone (P) and benzopyran (B) as π-linking groups were synthesized. The compounds exhibited aggregation-induced emission and piezochromic properties. Compared with previously reported donors, triphenylpyrroles induced all the compounds to have more remarkable photophysical properties. The compounds containing TPP-1,2,5 and P moieties displayed stronger fluorescence intensities, shorter emission wavelengths, and more distinct piezochromic properties. However, the same phenomenon was observed in the TPP-1,3,4-containing system if B was as π-linker. Moreover, the CN acceptor endowed the compound to have a relatively strong fluorescent intensity, in which CO induced a relatively long emission wavelength. That is, the photophysical properties of D–π–A compounds can be controlled by adjusting the structure of donor, linker and acceptor.

Visible-Light-Driven Synthesis of 1,3,4-Trisubstituted Pyrroles from Aryl Azides

Liu, Yang,Parodi, Adriano,Battaglioli, Simone,Monari, Magda,Protti, Stefano,Bandini, Marco

supporting information, p. 7782 - 7786 (2019/10/14)

The synthesis of 1,3,4-trisubstituted pyrroles via visible-light mediated photoredox catalyzed condensation of arylazides and aldehydes has been reported herein. The methodology avoids the use of stoichiometric oxidants and provides the corresponding N-co

Electrochemical oxidative annulation of amines and aldehydes or ketones to synthesize polysubstituted pyrroles

Gao, Xinlong,Wang, Pan,Wang, Qingqing,Chen, Jingting,Lei, Aiwen

supporting information, p. 4941 - 4945 (2019/09/30)

A general and practical protocol to synthesize polysubstituted pyrroles has been established by electrooxidative annulation of amines and aldehydes or ketones. In an undivided cell, arylacetaldehydes and primary amines can participate in this transformati

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