2199-93-1 Usage
Uses
Used in Pharmaceutical Industry:
3-acetyl-6-bromo-2H-chromen-2-one is used as a bioactive molecule for its anti-inflammatory properties, offering potential therapeutic benefits in treating inflammation-related conditions.
3-acetyl-6-bromo-2H-chromen-2-one is also used as an anti-tumor agent, targeting various types of cancer cells and potentially enhancing the efficacy of conventional cancer treatments.
Used in Antimicrobial Applications:
In the field of antimicrobial research, 3-acetyl-6-bromo-2H-chromen-2-one is utilized for its antimicrobial properties, providing a potential alternative to conventional antibiotics in combating resistant bacterial strains.
Used in Antioxidant Formulations:
3-acetyl-6-bromo-2H-chromen-2-one is employed as an antioxidant in various formulations, leveraging its ability to neutralize free radicals and protect cells from oxidative damage, which is crucial in skincare and health supplement industries.
Used in Organic Chemistry:
As a versatile precursor in organic chemistry, 3-acetyl-6-bromo-2H-chromen-2-one is used in the synthesis of other bioactive molecules and pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 2199-93-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,9 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2199-93:
(6*2)+(5*1)+(4*9)+(3*9)+(2*9)+(1*3)=101
101 % 10 = 1
So 2199-93-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H7BrO3/c1-6(13)9-5-7-4-8(12)2-3-10(7)15-11(9)14/h2-5H,1H3
2199-93-1Relevant academic research and scientific papers
The chameleon-like behaviour of 3-amino-1,2,4-triazole in the Biginelli reaction: Unexpected formation of a novel spiroheterocyclic system
Světlík, Jan,Kettmann, Viktor
experimental part, p. 1062 - 1066 (2011/03/22)
A novel Biginelli-like assembly of 3-amino-1,2,4-triazole with methyl acetoacetate and salicylaldehyde has been developed to enable easy access to spiro{[1]benzopyran-2,7′-[1,2,4]triazolo[1,5-a]pyrimidine} compounds as representatives of a new class of sp
