863870-99-9 Usage
Uses
Used in Pharmaceutical Industry:
2,4-DIPHENYLBENZOFURAN is used as a starting material for the synthesis of various organic compounds, facilitating the development of new pharmaceuticals. Its unique structure contributes to the creation of molecules with potential therapeutic properties.
Used in Agricultural Industry:
In agriculture, 2,4-DIPHENYLBENZOFURAN is utilized as a precursor in the production of agrochemicals, helping to develop compounds that can enhance crop protection and yield.
Used in Material Science:
2,4-DIPHENYLBENZOFURAN is employed as a building block in material science, contributing to the development of new materials with specific properties for various applications.
Used in Production of Fluorescent Dyes and Pigments:
2,4-DIPHENYLBENZOFURAN is used as a key component in the synthesis of fluorescent dyes and pigments, known for their bright and distinctive coloration, which is valuable in a range of industries including cosmetics, textiles, and art.
Used in Organic Electronics:
2,4-DIPHENYLBENZOFURAN is also studied for its potential use in organic electronics, where its properties may contribute to the development of novel electronic devices and components.
Used as a Potential Therapeutic Agent:
2,4-DIPHENYLBENZOFURAN has been investigated for its potential as a therapeutic agent for the treatment of various medical conditions, highlighting its versatility and importance in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 863870-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,8,7 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 863870-99:
(8*8)+(7*6)+(6*3)+(5*8)+(4*7)+(3*0)+(2*9)+(1*9)=219
219 % 10 = 9
So 863870-99-9 is a valid CAS Registry Number.
863870-99-9Relevant academic research and scientific papers
A new and efficient synthesis of 4-functionalized benzo[6]furans from 2,3-dihalophenols
Sanz, Roberto,Castroviejo, M. Pilar,Fernandez, Yolanda,Fananas, Francisco J.
, p. 6548 - 6551 (2007/10/03)
Tandem Sonogashira coupling/5-endo-dig cyclization reactions on 2,3-dihalophenols suppose a straightforward entry to 4-halobenzo[b]furans, which can be easily transformed into 4-functionalized benzo[b]furans, that are difficult to synthesize by other proc
