7154-63-4 Usage
Chromenyl group
A heterocyclic aromatic compound with a benzene ring and an oxygen atom.
Isoindole-1,3(2H)-dione group
A bicyclic compound with a fused indole ring and a carbonyl group.
Phenyl bridge
A benzene ring connecting the two main chemical groups.
Anti-inflammatory
The compound may help reduce inflammation in the body.
Antioxidant
The compound may help protect cells from damage caused by free radicals and oxidative stress.
Drug development
The compound's structural features make it a potential candidate for the development of new drugs.
Treatment of inflammation-related diseases
The compound's anti-inflammatory properties may be useful in treating conditions such as arthritis, asthma, and inflammatory bowel disease.
Treatment of oxidative stress-related diseases
The compound's antioxidant properties may be beneficial in treating conditions such as neurodegenerative diseases, cardiovascular diseases, and cancer.
Biological effects
More studies are needed to understand the compound's effects on living organisms and its potential therapeutic applications.
Potential applications
Further research is required to determine the compound's efficacy and safety in treating various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 7154-63-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7154-63:
(6*7)+(5*1)+(4*5)+(3*4)+(2*6)+(1*3)=94
94 % 10 = 4
So 7154-63-4 is a valid CAS Registry Number.
7154-63-4Relevant academic research and scientific papers
STEREOSELECTIVITY AT BENZYLIC CARBON. FLAVANOIDS-V. SYNTHESIS OF TRANS-4-ACETAMIDOFLAVANS
Hirwe, A.,Marathe, K. G.,Mohorkar, S. S.,Ramdas, K.,Singh, C. B.
, p. 1539 - 1546 (2007/10/02)
Some reactions of 4-substituted flavans have been studied. 4-Chloro/bromo derivatives react under neutral conditions with phthalimide and acetonitrile leading to displacement of axial halogen by nitrogen with inversion.In contrast, irrespective of the ste