1429431-66-2 Usage
Derivative of
Indole
Functional Groups
Chlorobenzyl group (C6H4Cl) attached to N-3 position of the indole ring
Two methyl groups (CH3) at the 2 and 3 positions of the indole ring
Potential Applications
Pharmaceutical industry: Potential drug candidate due to its unique structure and potential biological activity.
Agricultural industry: Potential pesticide candidate due to its structural features.
Interest for Further Research and Development
Unique structure and functional groups make it a subject of interest for further studies.
Requires additional research to fully understand and exploit its properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1429431-66-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,9,4,3 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1429431-66:
(9*1)+(8*4)+(7*2)+(6*9)+(5*4)+(4*3)+(3*1)+(2*6)+(1*6)=162
162 % 10 = 2
So 1429431-66-2 is a valid CAS Registry Number.
1429431-66-2Relevant articles and documents
Synthesis of 3,3′-Disubstituted Indolenines Utilizing the Lewis Acid Catalyzed Alkylation of 2,3-Disubstituted Indoles with Trichloroacetimidates
Adhikari, Arijit A.,Radal, Léa,Chisholm, John D.
supporting information, p. 2335 - 2339 (2017/10/06)
Trichloroacetimidates function as effective electrophiles for the selective C3-alkylation of 2,3-disubstituted indoles to provide 3,3′-disubstituted indolenines. These indolenines are common synthetic intermediates that are often utilized in the synthesis of complex molecules. Effective reaction conditions utilizing Lewis acid catalysts have been determined, and the scope of the reaction with respect to indole and imidate reaction partner has been investigated. This chemistry provides an alternative to base promoted and transition-metal-catalyzed methods that are more commonly utilized to access similar indolenines.
