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2-(4-(pentyloxy)phenyl)-1H-indole is an organic compound characterized by a unique molecular structure. It features an indole ring, which is a bicyclic structure consisting of a benzene ring fused to a pyrrole ring. The indole is substituted at the 2-position with a phenyl group, which in turn is connected to a pentyloxy chain at the 4-position. This pentyloxy group is an alkyl chain with five carbon atoms attached to an oxygen atom, which is then bonded to the phenyl ring. The compound's molecular formula is C20H23NO, indicating the presence of twenty carbon atoms, twenty-three hydrogen atoms, one nitrogen atom, and one oxygen atom. This chemical is known for its potential applications in the pharmaceutical and chemical industries, particularly in the synthesis of certain drugs and as a building block for more complex organic molecules.

5883-89-6

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5883-89-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5883-89-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,8 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5883-89:
(6*5)+(5*8)+(4*8)+(3*3)+(2*8)+(1*9)=136
136 % 10 = 6
So 5883-89-6 is a valid CAS Registry Number.

5883-89-6Downstream Products

5883-89-6Relevant academic research and scientific papers

Gold(i)-catalyzed synthesis of 2-substituted indoles from 2-alkynylnitroarenes with diboron as reductant

Fu, Wenqiang,Yang, Kai,Chen, Jinglong,Song, Qiuling

, p. 8354 - 8360 (2017/10/19)

An efficient method for the synthesis of 2-substituted indoles via a diboron/base promoted tandem reductive cyclization of o-alkynylnitroarene under Au catalysis conditions has been disclosed. This reaction is efficient and convenient, affording 2-substituted indoles with broad functional groups tolerance and excellent yields.

Antibacterial activity of a novel series of 3-bromo-4-(1H-3-indolyl)-2,5-dihydro-1H-2,5-pyrroledione derivatives - An extended structure-activity relationship study

Mahboobi, Siavosh,Eichhorn, Emerich,Winkler, Matthias,Sellmer, Andreas,Moellmann, Ute

, p. 633 - 656 (2008/09/19)

Compounds containing 3-bromo-2,5-dihydro-1H-2,5-pyrroledione and indole substructures were found to have antibacterial activity against resistant strains of Staphylococcus aureus and some other Gram positive bacteria. The investigated compounds exhibit mi

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