141306-15-2 Usage
Molecular structure
1H-Indole, 5-fluoro-3-(4-fluorophenyl)-1-(4-pyridinyl)is a complex molecule containing an indole core, fluorine, phenyl, and pyridine moieties.
Fluorine content
The presence of fluorine atoms in the molecule enhances its pharmaceutical properties and potential biological activities.
Pyridine moiety
The presence of a pyridine ring in the molecule adds to its structural complexity and may influence its potential applications in drug development.
Indole derivative
1H-Indole, 5-fluoro-3-(4-fluorophenyl)-1-(4-pyridinyl)- belongs to the class of indole derivatives, which are known for their diverse biological activities and potential applications in pharmaceuticals.
Pharmaceutical applications
1H-Indole, 5-fluoro-3-(4-fluorophenyl)-1-(4-pyridinyl)is used in the field of pharmaceuticals for the development of new drugs.
Drug discovery and development
The unique structural features and potential pharmacological effects of 1H-Indole, 5-fluoro-3-(4-fluorophenyl)-1-(4-pyridinyl)- make it a promising candidate for further research and studies in drug discovery and development.
Potential mechanisms of action
Further research may reveal specific uses and mechanisms of action for 1H-Indole, 5-fluoro-3-(4-fluorophenyl)-1-(4-pyridinyl)- in the medical field, potentially leading to the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 141306-15-2 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 141306-15:
(8*1)+(7*4)+(6*1)+(5*3)+(4*0)+(3*6)+(2*1)+(1*5)=82
82 % 10 = 2
So 141306-15-2 is a valid CAS Registry Number.
141306-15-2Relevant 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
