94481-79-5 Usage
Uses
Used in Pharmaceutical Industry:
(6S,7aS)-6-hydroxy-7,7a-dihydro-1-benzofuran-2(6H)-one is used as a building block for the synthesis of complex molecules and pharmaceuticals due to its unique structure and properties, which contribute to the development of novel drugs with potential therapeutic applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (6S,7aS)-6-hydroxy-7,7a-dihydro-1-benzofuran-2(6H)-one is utilized for its potential biological activities, which include antioxidant and anti-inflammatory properties. These characteristics make it a promising candidate for the development of new therapeutic agents targeting various health-related conditions.
Used in Antioxidant Applications:
(6S,7aS)-6-hydroxy-7,7a-dihydro-1-benzofuran-2(6H)-one is used as an antioxidant agent for its potential to combat oxidative stress and protect cells from damage, which is crucial in the prevention and treatment of various diseases and health conditions.
Used in Anti-inflammatory Applications:
(6S,7aS)-6-hydroxy-7,7a-dihydro-1-benzofuran-2(6H)-one is also used as an anti-inflammatory agent, leveraging its potential to reduce inflammation and alleviate symptoms associated with inflammatory diseases, thus contributing to the development of new treatments for such conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 94481-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,4,8 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 94481-79:
(7*9)+(6*4)+(5*4)+(4*8)+(3*1)+(2*7)+(1*9)=165
165 % 10 = 5
So 94481-79-5 is a valid CAS Registry Number.
94481-79-5Relevant academic research and scientific papers
Fluorescence study on the nyctinasty of Phyllanthus urinaria L. using novel fluorescence-labeled probe compounds
Kato, Nobuki,Inada, Masayoshi,Sato, Hirotaka,Miyatake, Ryoji,Kumagai, Tsutomu,Ueda, Minoru
, p. 7307 - 7318 (2007/10/03)
We report the synthesis of fluorescence-labeled probes based on phyllanthurinolactone 1, which is a leaf-closing substance of Phyllanthus urinaria L. The fluorescence study using biologically active probe 2 and inactive probes (epi-2 and 31) revealed that
