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1-(3,5-dimethylphenyl)-2-phenyl-1H-pyrrole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

940959-16-0

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940959-16-0 Usage

Class

Heterocyclic aromatic compound

Subclass

Pyrrole class of chemicals

Usage

Building block for charge-transporting materials in organic semiconductor devices

Properties

a. Excellent charge-transport properties
b. Thermal stability
c. Solubility

Applications

a. Organic solar cells
b. Organic light-emitting diodes (OLEDs)
c. Organic field-effect transistors (OFETs)

Potential therapeutic applications

Treating various diseases, including cancer and neurodegenerative disorders

Check Digit Verification of cas no

The CAS Registry Mumber 940959-16-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,0,9,5 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 940959-16:
(8*9)+(7*4)+(6*0)+(5*9)+(4*5)+(3*9)+(2*1)+(1*6)=200
200 % 10 = 0
So 940959-16-0 is a valid CAS Registry Number.

940959-16-0Downstream Products

940959-16-0Relevant academic research and scientific papers

Synthesis of polysubstituted pyrroles via Pd-catalyzed oxidative alkene C-H bond arylation and amination

Zheng, Jia,Huang, Liangbin,Huang, Chuyu,Wu, Wanqing,Jiang, Huanfeng

, p. 1235 - 1242 (2015)

A novel Pd(II)-catalyzed oxidative approach to construct polysubstituted pyrroles from N-homoallylicamines and arylboronic acids was developed. This transformation is supposed to proceed through cascade formation of C-C and C-N bonds via oxidative arylation of unactive alkenes, followed by intramolecular aza-Wacker cyclization.

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