47465-97-4 Usage
Description
3,3-Bis(3-methyl-4-hydroxyphenyl)indoline-2-on, also known as Bis(3-methyl-4-hydroxyphenyl)indoline, is an organic compound with the chemical formula C22H21NO2. It is a white solid and is known for its potential applications in various industries due to its unique chemical properties.
Uses
Used in Plastics Industry:
3,3-Bis(3-methyl-4-hydroxyphenyl)indoline-2-on is used as a material for polycarbonates for its ability to enhance the properties of the final product. Its incorporation into polycarbonate materials can improve characteristics such as strength, durability, and heat resistance, making it a valuable additive in the plastics industry.
Used in Pharmaceutical Industry:
While the provided materials do not explicitly mention pharmaceutical applications, the compound's chemical structure suggests potential use in the development of new drugs or as an intermediate in the synthesis of pharmaceutical compounds. Its hydroxy and aromatic groups could be exploited for interactions with biological targets, potentially leading to applications in drug discovery and development.
Used in Chemical Research:
3,3-Bis(3-methyl-4-hydroxyphenyl)indoline-2-on, due to its unique structure and properties, can be used as a subject of study in chemical research. Scientists may investigate its reactivity, stability, and potential to form new compounds or materials with novel properties. This could lead to the discovery of new applications in various fields, including materials science, electronics, and more.
Check Digit Verification of cas no
The CAS Registry Mumber 47465-97-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,4,6 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 47465-97:
(7*4)+(6*7)+(5*4)+(4*6)+(3*5)+(2*9)+(1*7)=154
154 % 10 = 4
So 47465-97-4 is a valid CAS Registry Number.
InChI:InChI=1/C22H19NO3/c1-13-11-15(7-9-19(13)24)22(16-8-10-20(25)14(2)12-16)17-5-3-4-6-18(17)23-21(22)26/h3-12,24-25H,1-2H3,(H,23,26)
47465-97-4Relevant articles and documents
Lambert Salt-Initiated Development of Friedel–Crafts Reaction on Isatin to Access Distinct Derivatives of Oxindoles
Khan, Jabir,Tyagi, Aparna,Yadav, Naveen,Mahato, Rina,Hazra, Chinmoy K.
, p. 17833 - 17847 (2021/12/17)
Herein, a mild metal-free and efficacious route for the synthesis of biologically important 3-aryl oxindole derivatives is described. Using Lambert salt-initiated hydroarylation of isatin, a diverse array of monoarylated products, symmetrical/unsymmetrical double-arylated products, and deoxygenated hydroarylated products could be synthesized from the single starting substrate in good to excellent yields. A preliminary mechanistic study revealed that the reaction proceeds via a monoarylated product followed by a nucleophilic attack by another electron-rich arene nucleophile under mild conditions. The potential of newly synthesized symmetric/unsymmetric 3,3-disubstituted oxindole, 3-substituted 3-hydroxy oxindoles, 3,3-di(indolyl)indolin-2-ones, and α-aryl oxindoles as valuable building blocks is further illustrated.
