18446-70-3 Usage
Description
(3aS)-6,9a-dimethyl-3-methylidene-3,3a,4,5,6,8,9a,9b-octahydroazuleno[4,5-b]furan-2,9-dione is a complex diterpenoid lactone with a molecular formula C15H18O3. It is often found in natural sources such as plants and fungi and has been studied for its potential bioactive properties, including anti-inflammatory, anti-cancer, and antimicrobial effects. Its unique chemical structure and potential medicinal properties make it an interesting target for further research and potential pharmaceutical development.
Uses
Used in Pharmaceutical Industry:
(3aS)-6,9a-dimethyl-3-methylidene-3,3a,4,5,6,8,9a,9b-octahydroazuleno[4,5-b]furan-2,9-dione is used as a potential pharmaceutical candidate for its anti-inflammatory, anti-cancer, and antimicrobial properties. Its unique chemical structure and bioactive properties make it a promising compound for the development of new drugs and therapies.
Used in Cosmetic Industry:
(3aS)-6,9a-dimethyl-3-methylidene-3,3a,4,5,6,8,9a,9b-octahydroazuleno[4,5-b]furan-2,9-dione can be used as an active ingredient in cosmetic products for its anti-inflammatory and antimicrobial properties. It may help to soothe and protect the skin, making it a valuable addition to skincare formulations.
Used in Agricultural Industry:
(3aS)-6,9a-dimethyl-3-methylidene-3,3a,4,5,6,8,9a,9b-octahydroazuleno[4,5-b]furan-2,9-dione may also have potential applications in the agricultural industry as a natural antimicrobial agent. It could be used to protect crops from bacterial and fungal infections, promoting healthy growth and reducing the need for chemical pesticides.
Check Digit Verification of cas no
The CAS Registry Mumber 18446-70-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,4 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 18446-70:
(7*1)+(6*8)+(5*4)+(4*4)+(3*6)+(2*7)+(1*0)=123
123 % 10 = 3
So 18446-70-3 is a valid CAS Registry Number.
18446-70-3Relevant articles and documents
Chemical and Biochemical Modifications of Parthenin
Das, Biswanath,Venkataiah, B.,Kashinatham, A.
, p. 6585 - 6594 (2007/10/03)
Parthenin, a medicinally important natural sesquiterpenoid and a potent allelochemical underwent different regio- and stereoselective modifications to several interesting analogues by chemical and biochemical means. The compound was treated with various common reducing agents including NaBH4, NaBH4/I2, Na/EtOH, Mg/MeOH and Zn/HOAc as well as with different oxidizing agents including m-CPBA and dilute HCl under different reaction conditions. The retention of the α-methylene-γ-lactone moiety which plays a vital role for bioactivity of the compound was observed in some of the reaction products. The microwave irradiation of the compound afforded anhydroparthenin as the only product. Baker's yeast reduction of parthenin was investigated for the first time and yielded the naturally occurring dihydrocoronopilin. - Keywords: parthenin, sesquiterpenoid, α-methylene-γ-lactone, chemical modifications, baker's yeast reduction.
Enantioselective synthesis of neoambrosin, parthenin, and dihydroisoparthenin
Asaoka, Morio,Ohkubo, Taketoshi,Itahana, Hirotsune,Kosaka, Takatoshi,Takei, Hisashi
, p. 3115 - 3128 (2007/10/02)
Enantioselective synthesis of the titled ambrosanolides is described. Use of the trimethylsilyl group as an anchor contributed to the stereoselective introduction of two methyl groups.