141306-86-7 Usage
Methyl ester derivative
1H-Indole-2-carboxylic acid, 6-chloro-3-(4-fluorophenyl)This indicates that the compound is derived from 1H-Indole-2-carboxylic acid by replacing the hydrogen atom on the carboxylic acid group with a methyl group.
Class of compounds
Indole carboxylic acid derivatives This indicates that the compound belongs to a group of compounds that have similar chemical and pharmacological properties.
Pharmacological activities
Known for their pharmacological activities This suggests that the compound may have potential therapeutic uses.
Industrial applications
Used as an intermediate in the synthesis of pharmaceutical compounds and agrochemicals This indicates that the compound is used in the production of other chemicals that have practical applications in the pharmaceutical and agricultural industries.
Chemical properties
Presence of chlorine and fluorine The presence of these halogen atoms may affect the reactivity and stability of the compound.
Biological properties
Potentially impart specific chemical and biological properties The presence of chlorine and fluorine may also affect the compound's interactions with biological systems, making it valuable in research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 141306-86-7 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, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 141306-86:
(8*1)+(7*4)+(6*1)+(5*3)+(4*0)+(3*6)+(2*8)+(1*6)=97
97 % 10 = 7
So 141306-86-7 is a valid CAS Registry Number.
141306-86-7Relevant 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
