60821-63-8 Usage
Uses
Used in Pharmaceutical Industry:
1-(2,3-dihydro-1-Methyl-1H-indol-5-yl)-Ethanone is used as an intermediate compound for the synthesis of various pharmaceuticals. Its application is primarily due to its potential medicinal properties, which have been studied for treating a range of diseases and disorders.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(2,3-dihydro-1-Methyl-1H-indol-5-yl)-Ethanone is used as a key component in the development of various agrochemical products. Its usage stems from its ability to be synthesized into compounds that can be applied in the agricultural sector for pest control and other related purposes.
Used in Organic Synthesis:
1-(2,3-dihydro-1-Methyl-1H-indol-5-yl)-Ethanone is utilized as a vital component in organic synthesis. Its unique structure allows it to be a versatile building block for the creation of a wide array of organic compounds, making it an indispensable tool for researchers in the field of chemistry.
Used in Research:
1-(2,3-dihydro-1-Methyl-1H-indol-5-yl)-Ethanone is also used as a research tool, particularly in the fields of chemistry and pharmacology. Its distinctive properties and structure make it an attractive subject for scientific investigations, potentially leading to the discovery of new applications and uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 60821-63-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,2 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60821-63:
(7*6)+(6*0)+(5*8)+(4*2)+(3*1)+(2*6)+(1*3)=108
108 % 10 = 8
So 60821-63-8 is a valid CAS Registry Number.
60821-63-8Relevant articles and documents
Acetylation of N-heteroaryl bromides via PdCl2/(o-tolyl) 3P catalyzed heck reactions
He, Tianxiong,Tao, Xiaochun,Wu, Xinyan,Cai, Lisheng,Pike, Victor W.
, p. 887 - 890 (2008/09/21)
A new user-friendly and convenient method for the acetylation of N-heteroaryl bromides is described. This process is based on the palladium-catalyzed olefination of an N-heteroaryl bromide with butyl vinyl ether, followed by acid hydrolysis of the intermediate heteroaryl vinyl ether in situ. Isopropanol at 85°C, in the presence of K3PO 4·3H2O (2 equiv), PdCl2 (2 mol%) and (o-tolyl)3P (4 mol%), provided the best conditions, giving yields of N-heteroaryl bromides up to 75%. Georg Thieme Verlag Stuttgart.
