76777-56-5 Usage
Uses
Used in Flavoring and Food Industry:
2,2-dimethyl-5-(prop-1-en-2-yl)furan-3(2H)-one is used as a flavoring agent for its sweet, fruity odor, enhancing the taste and aroma of food and beverages. Its natural occurrence in certain foods contributes to its acceptability and appeal in the culinary world.
Used in Fragrance Industry:
In the fragrance industry, 2,2-dimethyl-5-(prop-1-en-2-yl)furan-3(2H)-one is used as a component to add a sweet, fruity note to perfumes and cosmetic products, capitalizing on its pleasant and distinctive scent profile.
Used in Pharmaceutical and Nutraceutical Applications:
Given its antioxidant, anti-inflammatory, and anticancer properties, 2,2-dimethyl-5-(prop-1-en-2-yl)furan-3(2H)-one is explored for potential use in pharmaceutical and nutraceutical products to support health and wellness.
Used in Cosmetic Products:
Due to its natural presence in various plants and its biological activities, 2,2-dimethyl-5-(prop-1-en-2-yl)furan-3(2H)-one may also be utilized in cosmetic products for its potential skin health benefits, such as anti-inflammatory and antioxidant effects.
Check Digit Verification of cas no
The CAS Registry Mumber 76777-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,7,7 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 76777-56:
(7*7)+(6*6)+(5*7)+(4*7)+(3*7)+(2*5)+(1*6)=185
185 % 10 = 5
So 76777-56-5 is a valid CAS Registry Number.
76777-56-5Relevant academic research and scientific papers
New 5-(2-ethenylsubstituted)-3(2H)-furanones with in vitro antiproliferative activity
Chimichi, Stefano,Boccalini, Marco,Cosimelli, Barbara,Dall'Acqua, Francesco,Viola, Giampietro
, p. 5215 - 5223 (2007/10/03)
A convenient route to new 3(2H)-furanones is described through hydrogenolysis and subsequent acidic hydrolysis of isoxazoles. The antiproliferative activity of title compounds were evaluated against leukemia-, carcinoma-, neuroblastoma-, and sarcoma-derived human cell lines in comparison to the natural compound geiparvarin. The structure activity relationship indicated that the maximum in vitro antiproliferative activity correlates with the presence of a heterocyclic ring on the ethenyl moiety.
Synthesis and Reactions of Simple 3(2H)-Furanones
Smith, Amos B.,Levenberg, Patricia A.,Jerris, Paula J.,Scarborough, Robert M.,Wovkulich, Peter M.
, p. 1501 - 1513 (2007/10/02)
Interest in the total synthesis of natural product antitumor agents which have as a central structural element the 3(2H)-furanone ring system has led to the development of an efficient general synthesis of a variety of simple 3(2H)-furanones.The strategy
