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1H-Indole, 3-(4-fluorophenyl)-1-(4-pyridinyl)-5-(trifluoromethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

141306-17-4

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141306-17-4 Usage

Core structure

1H-Indole
A bicyclic organic compound consisting of a 6-membered benzene ring fused to a 5-membered nitrogen-containing pyrrole ring.

1-(4-pyridinyl)

A pyridinyl group, which is a 6-membered nitrogen-containing ring with five carbon atoms, attached at the 1-position of the indole core. This group has a hydrogen atom replaced by a methyl group at the 4-position.

Pharmaceutical and agrochemical research

The compound is used to study its potential biological activities, which may lead to the development of new drugs or agrochemicals.

Medicinal chemistry

The compound serves as a building block for the synthesis of various biologically active compounds, contributing to the development of new therapeutic agents.

Drug candidate potential

The specific structural features of the compound may make it a promising candidate for the treatment of various diseases, depending on its demonstrated biological activities and further research.

Check Digit Verification of cas no

The CAS Registry Mumber 141306-17-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,3,0 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 141306-17:
(8*1)+(7*4)+(6*1)+(5*3)+(4*0)+(3*6)+(2*1)+(1*7)=84
84 % 10 = 4
So 141306-17-4 is a valid CAS Registry Number.

141306-17-4Relevant academic research and scientific papers

Selective, Centrally Acting Serotonin 5-HT2 Antagonists. 2. Substituted 3-(4-Fluorophenyl)-1H-indoles

Andersen, Kim,Perregaard, Jens,Arnt, Joern,Nielsen, Joern Bay,Begtrup, Mikael

, p. 4823 - 4831 (2007/10/02)

A series of 3-(4-fluorophenyl)-1H-indoles substituted in the 1-position with 4-piperidinyl, 1,2,3,6-tetrahydro-4-pyridinyl, and 4-piperazinyl was synthesized. By variation of the substituents in the benzene part of the indole nucleus in 1-2-4-3-(4-fluo

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