57642-07-6 Usage
Description
1-(1H-indol-3-yl)-2-methylpropan-1-one, also known as 3-(1H-indol-3-yl)-2-methylpropan-1-one, is a chemical compound with the molecular formula C12H13NO. It is a derivative of indole, characterized by its unique structure that includes an indole ring and a ketone group. 1-(1H-indol-3-yl)-2-methylpropan-1-one is recognized for its potential biological and pharmacological activities, such as anti-inflammatory and antioxidant properties, and is utilized as a crucial building block in the synthesis of complex organic molecules.
Uses
Used in Pharmaceutical Industry:
1-(1H-indol-3-yl)-2-methylpropan-1-one is used as a precursor for the production of various pharmaceuticals. Its unique structure allows it to serve as an essential building block in the synthesis of a wide range of complex organic molecules, contributing to the development of new drugs with diverse therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(1H-indol-3-yl)-2-methylpropan-1-one is utilized as a starting material for the synthesis of different agrochemicals. Its chemical properties make it suitable for the creation of compounds that can be used in the development of pesticides, herbicides, and other agricultural products to enhance crop protection and yield.
Used in Organic Synthesis:
1-(1H-indol-3-yl)-2-methylpropan-1-one is also used in organic synthesis, where it plays a vital role in the formation of various complex organic molecules. Its indole ring and ketone group provide a versatile framework for chemical reactions, enabling the creation of a broad spectrum of organic compounds for different applications in research and industry.
Used in Biological and Pharmacological Research:
Due to its potential biological and pharmacological activities, including anti-inflammatory and antioxidant effects, 1-(1H-indol-3-yl)-2-methylpropan-1-one is used in research as a compound of interest. Scientists study its properties to understand its mechanisms of action and explore its potential for developing new therapeutic agents or improving existing ones.
Check Digit Verification of cas no
The CAS Registry Mumber 57642-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,4 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 57642-07:
(7*5)+(6*7)+(5*6)+(4*4)+(3*2)+(2*0)+(1*7)=136
136 % 10 = 6
So 57642-07-6 is a valid CAS Registry Number.
57642-07-6Relevant articles and documents
An efficient and green method for regio- and chemo-selective Friedel-Crafts acylations using a deep eutectic solvent ([CholineCl][ZnCl2]3)
Tran, Phuong Hoang,Nguyen, Hai Truong,Hansen, Poul Erik,Le, Thach Ngoc
, p. 37031 - 37038 (2016/05/24)
[CholineCl][ZnCl2]3, a deep eutectic solvent between choline chloride and ZnCl2, has been used as a dual function catalyst and green solvent for the Friedel-Crafts acylation of aromatic compounds instead of using the moisture-sensitive Lewis acids and volatile organic solvents. The reactions are performed with high yields under microwave irradiation with short reaction times for the synthesis of ketones. Interestingly, indole derivatives are regioselectively acylated in the 3-position under mild conditions with high yields without NH protection. Three new ketone products are synthesized. [CholineCl][ZnCl2]3 is easily synthesized from choline chloride and zinc chloride at a low cost, with easy purification and environmentally benign compounds. [CholineCl][ZnCl2]3 can be reused up to five times without loss of catalytic activity, making it ideal in industrial processes.
