1623751-93-8 Usage
Uses
Used in Pharmaceutical Industry:
(4-chlorophenyl)(1-methyl-1H-indol-7-yl)methanone is used as a potential pharmaceutical compound for its aromatic properties and carbonyl functional group, which may contribute to its interaction with biological targets and its potential use in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, (4-chlorophenyl)(1-methyl-1H-indol-7-yl)methanone may be utilized as a precursor or active ingredient in the development of pesticides or other agricultural chemicals, leveraging its chemical structure to target specific pests or enhance crop protection.
Used in Materials Science:
(4-chlorophenyl)(1-methyl-1H-indol-7-yl)methanone could be employed in materials science for the development of new materials with unique properties. Its aromatic and carbonyl characteristics might be harnessed to create novel polymers, coatings, or other advanced materials with specific applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1623751-93-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,3,7,5 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1623751-93:
(9*1)+(8*6)+(7*2)+(6*3)+(5*7)+(4*5)+(3*1)+(2*9)+(1*3)=168
168 % 10 = 8
So 1623751-93-8 is a valid CAS Registry Number.
1623751-93-8Relevant academic research and scientific papers
Rhodium enalcarbenoids: Direct synthesis of indoles by rhodium(II)- catalyzed [4+2] benzannulation of pyrroles
Dawande, Sudam Ganpat,Kanchupalli, Vinaykumar,Kalepu, Jagadeesh,Chennamsetti, Haribabu,Lad, Bapurao Sudam,Katukojvala, Sreenivas
, p. 4076 - 4080 (2014/05/06)
Disclosed herein is the design of an unprecedented electrophilic rhodium enalcarbenoid which results from rhodium(II)-catalyzed decomposition of a new class of enaldiazo compounds. The synthetic utility of these enalcarbenoids has been successfully demonstrated in the first transition-metal-catalyzed [4+2] benzannulation of pyrroles, thus leading to substituted indoles. The new benzannulation has been applied to the efficient synthesis of the natural product leiocarpone as well as a potent adipocyte fatty-acid binding protein inhibitor. Fat cat: A new class of enaldiazo compounds resulted in the first transition-metal-catalyzed [4+2] benzannulation of pyrroles to deliver indoles. The benzannulation is proposed to involve an unprecedented diacceptor rhodium enalcarbenoid. The reaction was used in the highly efficient synthesis of the natural product leiocarpone and a potent adipocyte fatty-acid binding protein inhibitor.
