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

141306-20-9

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141306-20-9 Usage

Molecular Structure

The compound has a 1H-indole core structure with a 4-fluorophenyl group attached at the 3-position and a piperidinyl group at the 1-position.

Chemical Class

It belongs to the class of indole derivatives.

Pharmacological Activities

The compound has potential pharmacological activities and may be used in medicinal chemistry research for the development of new drugs targeting relevant biological pathways.

Toxicological Effects

It may have potential toxicological effects and should be handled with caution.

Handling and Use

The compound should only be handled by qualified individuals in a controlled laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 141306-20-9 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, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 141306-20:
(8*1)+(7*4)+(6*1)+(5*3)+(4*0)+(3*6)+(2*2)+(1*0)=79
79 % 10 = 9
So 141306-20-9 is a valid CAS Registry Number.

141306-20-9Downstream Products

141306-20-9Relevant academic research and scientific papers

3-ARYLINDOLE COMPOUNDS

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, (2008/06/13)

3-Arylindole or 3-arylindazole derivatives having formula: STR1 wherein Ar is optionally substituted phenyl or a heteroaromatic group; R. sup.1-R 4 are independently selected from hydrogen, halogen, alkyl, alkoxy, hydroxy, nitro, alkylthio, alkylsulphonyl

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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