55249-44-0 Usage
Uses
Used in Pharmaceutical Industry:
(4E)-1a,5-dimethyl-8-methylidene-9-oxo-1a,2,3,6,7,7a,8,9,10a,10b-decahydrooxireno[9,10]cyclodeca[1,2-b]furan-6-yl acetate is used as a pharmaceutical compound for its potential therapeutic effects. Its unique structure may allow it to interact with biological targets in ways that could lead to the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical industry, (4E)-1a,5-dimethyl-8-methylidene-9-oxo-1a,2,3,6,7,7a,8,9,10a,10b-decahydrooxireno[9,10]cyclodeca[1,2-b]furan-6-yl acetate is used as an active ingredient in pesticides or herbicides. Its specific chemical properties might provide effective control over pests or unwanted plant growth.
Used in Synthesis of Other Compounds:
(4E)-1a,5-dimethyl-8-methylidene-9-oxo-1a,2,3,6,7,7a,8,9,10a,10b-decahydrooxireno[9,10]cyclodeca[1,2-b]furan-6-yl acetate serves as a key intermediate in the synthesis of other complex organic compounds. Its presence in a reaction may enable the creation of new molecules with diverse applications.
Further analysis and research are required to fully understand the potential uses and effects of (4E)-1a,5-dimethyl-8-methylidene-9-oxo-1a,2,3,6,7,7a,8,9,10a,10b-decahydrooxireno[9,10]cyclodeca[1,2-b]furan-6-yl acetate, as its complex nature may reveal additional applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 55249-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,4 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55249-44:
(7*5)+(6*5)+(5*2)+(4*4)+(3*9)+(2*4)+(1*4)=130
130 % 10 = 0
So 55249-44-0 is a valid CAS Registry Number.
55249-44-0Relevant academic research and scientific papers
Synthetic Modification of 9α- and 9β-Hydroxyparthenolide by Heck or Acylation Reactions and Evaluation of Cytotoxic Activities
El Bouakher, Abderrahman,Jismy, Badr,Allouchi, Hassan,Duverger, Eric,Barkaoui, Latifa,El Hakmaoui, Ahmed,Daniellou, Richard,Guillaumet, Gérald,Akssira, Mohamed
, p. 661 - 671 (2017/05/09)
Motivated by the widely reported anticancer activity of parthenolides and their derivatives, a series of new substituted parthenolides was efficiently synthesized. Structural modifications were performed at the C-9 and C-13 positions of 9α- and 9β-hydroxyparthenolide, which were isolated from the aerial parts of Anvillea radiata. Twenty-one derivatives were synthesized and evaluated for their in vitro cytotoxic activity against HS-683, SK-MEL-28, A549, and MCF-7 human cancer cell lines using the MTT colorimetric assay. Among the derivatives, seven exhibited excellent activity compared to 5-fluorouracil and etoposide against the four cell lines tested, with IC50 values ranging from 1.1 to 9.4 μM.
