4702-36-7 Usage
Uses
1H-2-Benzopyran-1-one,8-hydroxyis used as an antibiotic agent for the defense against bacterial infections. Its antibiotic properties make it a valuable compound in the development of new drugs to combat bacterial pathogens, particularly in the context of increasing antibiotic resistance.
Used in Pharmaceutical Industry:
1H-2-Benzopyran-1-one,8-hydroxyis used as a pharmaceutical compound for its potential therapeutic applications. 1H-2-Benzopyran-1-one,8-hydroxy-'s ability to exhibit antibiotic properties suggests that it could be a promising candidate for the development of new antibiotics to treat a range of bacterial infections. Additionally, its unique molecular structure may also offer opportunities for further research and development in other therapeutic areas.
Used in Research and Development:
1H-2-Benzopyran-1-one,8-hydroxyis used as a research compound for the investigation of its biological activities and potential applications. 1H-2-Benzopyran-1-one,8-hydroxy-'s antibiotic properties, as well as its unique molecular structure, make it an interesting subject for further study. Researchers may explore its potential use in the development of new drugs, as well as its interactions with various biological targets and pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 4702-36-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4702-36:
(6*4)+(5*7)+(4*0)+(3*2)+(2*3)+(1*6)=77
77 % 10 = 7
So 4702-36-7 is a valid CAS Registry Number.
4702-36-7Relevant academic research and scientific papers
Gold(I)-Catalyzed Cyclization for the Synthesis of 8-Hydroxy-3- substituted Isocoumarins: Total Synthesis of Exserolide F
Mallampudi, N. Arjunreddy,Reddy, G. Sudhakar,Maity, Saurabh,Mohapatra, Debendra K.
, p. 2074 - 2077 (2017/04/28)
A highly regioselective gold(I)-catalyzed 6-endo-dig cyclization of 2,2-dimethyl-5-(alkynyl)-4H-benzo[d][1,3]dioxin-4-ones for the synthesis of 8-hydroxy-3-substituted isocoumarins is described. Key features of the reaction include the broad substrate scope, scalability, and tolerance for protecting groups. The synthetic utility of this novel method is demonstrated by the first total synthesis of exserolide F, an isocoumarin-containing polyol natural product.
