141306-85-6 Usage
Methyl ester derivative
5-chloro-3-phenylindole-2-carboxylic acid This indicates that the compound is derived from 5-chloro-3-phenylindole-2-carboxylic acid and has an ester functional group.
Used in organic synthesis and pharmaceutical research
This suggests that the compound is commonly used in the synthesis of other compounds and in drug development.
Potential medicinal properties
This indicates that the compound has potential therapeutic uses and has been studied for its potential applications in drug development.
Valuable building block for the synthesis of various bioactive compounds
This suggests that the compound's structure, including an indole ring with a chlorine atom and a phenyl group, makes it useful for the synthesis of other bioactive compounds.
Methyl ester form adds flexibility to its use in various chemical reactions
This suggests that the compound's ester functional group allows it to be used in a wide range of chemical reactions and organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 141306-85-6 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 141306-85:
(8*1)+(7*4)+(6*1)+(5*3)+(4*0)+(3*6)+(2*8)+(1*5)=96
96 % 10 = 6
So 141306-85-6 is a valid CAS Registry Number.
141306-85-6Relevant academic research and scientific papers
Cleavage of C-C Bonds for the Synthesis of C2-Substituted Quinolines and Indoles by Catalyst-Controlled Tandem Annulation of 2-Vinylanilines and Alkynoates
Ni, Jixiang,Jiang, Yong,An, Zhenyu,Yan, Rulong
, p. 1534 - 1537 (2018/03/23)
The strategy for the synthesis of C2-substituted indoles and quinolines from 2-vinylanilines and alkynoates through C-C bond cleavage is developed. With these general methods, 2-substituted indoles and quinolines can be accessed via tandem Michael addition and cyclization with no requirement of oxidant. This strategy not only provides a method for the synthesis C2-substituted indoles in good yields through the simultaneous cleavage of C=C and C=C bonds under metal-free conditions but also provides a simple method for the generation of the C2-substituted quinolines in moderate yields via Pd-catalyzed C=C bond cleavage.
