187932-50-9 Usage
Description
6-Bromo-3'-nitroflavone is a flavone derivative, which belongs to the class of heterocyclic polyphenolic compounds. These compounds are extensively found in the plant kingdom and are recognized for their significant pharmaceutical, biocidal, and antioxidant properties.
Uses
Used in Pharmaceutical Applications:
6-Bromo-3'-nitroflavone is used as a pharmaceutical agent for its potential therapeutic effects. The compound's biocidal and antioxidant activities contribute to its value in the development of new drugs for various health conditions.
Used in Antioxidant Applications:
In the field of antioxidant applications, 6-bromo-3'-nitroflavone serves as a potent antioxidant, protecting cells from oxidative stress and damage, which can lead to various diseases and aging.
Used in Biocidal Applications:
6-Bromo-3'-nitroflavone is also utilized as a biocidal agent, leveraging its ability to combat harmful microorganisms and pests, making it a valuable component in the development of antimicrobial and antifungal products.
Used in Research and Development:
In the research and development industry, 6-bromo-3'-nitroflavone is used as a key compound for studying the structure-activity relationships of flavone derivatives, which can lead to the discovery of novel pharmaceuticals and biocides with improved properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 187932-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,7,9,3 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 187932-50:
(8*1)+(7*8)+(6*7)+(5*9)+(4*3)+(3*2)+(2*5)+(1*0)=179
179 % 10 = 9
So 187932-50-9 is a valid CAS Registry Number.
187932-50-9Relevant articles and documents
A two step synthesis of BzR/GABAergic active flavones via a Wacker-related oxidation
Lorenz, Michael,Shahjahan Kabir,Cook, James M.
experimental part, p. 1095 - 1098 (2010/04/05)
A general route for the synthesis of biologically important flavones is reported via a two step sequence employing a catalytic Wacker-Cook oxidation4b as the key step.
Use of nitroflavonoids for the treatment of anxiety
-
, (2008/06/13)
PCT No. PCT/GB96/02523 Sec. 371 Date Jul. 8, 1998 Sec. 102(e) Date Jul. 8, 1998 PCT Filed Oct. 16, 1996 PCT Pub. No. WO97/14414 PCT Pub. Date Apr. 24, 1997Methods of treating anxiety with flavonoid compounds according to Formula (I) and dimers thereof, co
