141306-65-2 Usage
Molecular weight
270.28 g/mol
Structure
1H-Indole-2-carboxylic acid, 3-(4-fluorophenyl)-, methyl ester
Appearance
Solid
Melting point
Not provided
Solubility
Not provided
Polarity
Polar
Functional groups
Carboxylic acid, ester, indole ring, fluorophenyl group
Uses
Building block in the synthesis of drugs with anti-inflammatory, analgesic, or anti-cancer properties
Form
Methyl ester for easier manipulation and synthesis of other organic molecules
Specific chemical properties
3-(4-fluorophenyl) group for targeting biological pathways or receptors in drug design
Potential applications
Pharmaceutical industry, materials science, chemical research
Check Digit Verification of cas no
The CAS Registry Mumber 141306-65-2 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, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141306-65:
(8*1)+(7*4)+(6*1)+(5*3)+(4*0)+(3*6)+(2*6)+(1*5)=92
92 % 10 = 2
So 141306-65-2 is a valid CAS Registry Number.
141306-65-2Relevant academic research and scientific papers
Synthesis and evaluation of 2-carboxy indole derivatives as potent and selective anti-leukemic agents
Cury, Nathália Moreno,Capit?o, Rebeca Monique,Almeida, Renan do Canto Borges de,Artico, Leonardo Luís,Corrêa, Juliana Ronchi,Sim?o dos Santos, Eric Francisco,Yunes, José Andrés,Correia, Carlos Roque Duarte
, (2019/08/12)
Despite the success achieved in the treatment of acute lymphoblastic leukemia (ALL), the search for new drugs featuring selectivity against leukemia cells and effectiveness to prevent relapsed ALL is still highly desirable. Here, we described the synthesi
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
