6307-94-4 Usage
Molecular Structure
The compound has a complex structure consisting of a benzofuran core with a substituted benzylidene group and a methoxy group.
Usage in Pharmaceutical Research
It is commonly used in pharmaceutical research due to its potential medicinal properties.
Applications in Drug Discovery and Development
The compound is particularly useful in the field of drug discovery and development.
Antioxidant Properties
2-(4-hydroxy-3-methoxybenzylidene)-7-methoxy-1-benzofuran-3(2H)-one has been studied for its antioxidant activities.
Anti-inflammatory Properties
The compound has been studied for its anti-inflammatory activities.
Antimicrobial Properties
2-(4-hydroxy-3-methoxybenzylidene)-7-methoxy-1-benzofuran-3(2H)-one has been studied for its antimicrobial activities.
Potential Treatment of Various Diseases
Due to its multiple properties, it is a potential candidate for the treatment of various diseases.
Applications in Cosmetic and Food Industries
The compound may have applications in the cosmetic and food industries for its antioxidant properties.
Versatile Compound
2-(4-hydroxy-3-methoxybenzylidene)-7-methoxy-1-benzofuran-3(2H)-one is a versatile compound.
Promising Therapeutic and Commercial Potential
The compound has promising therapeutic and commercial potential.
Check Digit Verification of cas no
The CAS Registry Mumber 6307-94-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6307-94:
(6*6)+(5*3)+(4*0)+(3*7)+(2*9)+(1*4)=94
94 % 10 = 4
So 6307-94-4 is a valid CAS Registry Number.
6307-94-4Relevant academic research and scientific papers
Design and synthesis of 4β-Acetamidobenzofuranone-podophyllotoxin hybrids and their anti-cancer evaluation
Paidakula, Suresh,Nerella, Srinivas,Vadde, Ravinder,Kamal,Kankala, Shravankumar
supporting information, p. 2153 - 2156 (2019/07/08)
A new series of amide derivatives of 4β-Acetamidobenzofuranone-podophyllotoxin hybrids (14a–g) were synthesized and their chemical structures were confirmed by 1H, 13C NMR and mass spectral data. Further, all the synthesized Acetamid
