3306-52-3 Usage
Uses
Used in Pharmaceutical Applications:
[1S-(1alpha,2alpha,11balpha)]-1,7,8,11b-tetrahydro-1-hydroxy-2-methoxy-11b-methylcyclopenta[7,8]phenanthro[10,1-bc]furan-3,6,9(2H)-trione is used as a potential therapeutic agent for various medical conditions due to its complex structure and the presence of functional groups that may interact with biological targets.
Used in Chemical Research:
[1S-(1alpha,2alpha,11balpha)]-1,7,8,11b-tetrahydro-1-hydroxy-2-methoxy-11b-methylcyclopenta[7,8]phenanthro[10,1-bc]furan-3,6,9(2H)-trione is utilized as a subject of study in chemical research to understand its reactivity, stability, and the possibility of its use as a building block for the synthesis of other complex molecules with potential applications in different industries.
Used in Drug Delivery Systems:
Similar to gallotannin, [1S-(1alpha,2alpha,11balpha)]-1,7,8,11b-tetrahydro-1-hydroxy-2-methoxy-11b-methylcyclopenta[7,8]phenanthro[10,1-bc]furan-3,6,9(2H)-trione could be employed in the development of novel drug delivery systems. Its unique structure might allow for the creation of targeted drug carriers that could improve the bioavailability and efficacy of various pharmaceuticals.
Used in Material Science:
[1S-(1alpha,2alpha,11balpha)]-1,7,8,11b-tetrahydro-1-hydroxy-2-methoxy-11b-methylcyclopenta[7,8]phenanthro[10,1-bc]furan-3,6,9(2H)-trione's structural features may also find applications in material science, where it could be investigated for its potential use in the development of new materials with specific properties, such as improved strength, flexibility, or chemical resistance.
Used in Environmental Applications:
Given its complex structure and functional groups, this chemical might also be studied for its potential use in environmental applications, such as a component in the remediation of pollutants or as a part of green chemistry initiatives.
Check Digit Verification of cas no
The CAS Registry Mumber 3306-52-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3306-52:
(6*3)+(5*3)+(4*0)+(3*6)+(2*5)+(1*2)=63
63 % 10 = 3
So 3306-52-3 is a valid CAS Registry Number.
3306-52-3Relevant academic research and scientific papers
Total Synthesis of Viridin and Viridiol
Ji, Yang,Xin, Zhengyuan,He, Haibing,Gao, Shuanhu
supporting information, p. 16208 - 16212 (2019/10/14)
The asymmetric total synthesis of (-)-viridin and (-)-viridiol, antifungal metabolites, was achieved in 17 and 18 steps from a commercially available starting material. An intramolecular [3+2] cycloaddition was applied to an easily available l-ribose derivative in order to construct the highly substituted D ring containing the key chiral cis-triol fragment. Co-catalyzed metal-hydride H atom transfer (MHAT) radical cyclization was utilized to form the C-ring and the all-carbon quaternary center at C-10. This convergent strategy provides a scalable approach to prepare viridin and viridiol for biological studies.
Enantioselective Chemical Syntheses of the Furanosteroids (-)-Viridin and (-)-Viridiol
Del Bel, Matthew,Abela, Alexander R.,Ng, Jeffrey D.,Guerrero, Carlos A.
supporting information, p. 6819 - 6822 (2017/05/31)
Herein we describe concise enantioselective chemical syntheses of (-)-viridin and (-)-viridiol. Our convergent approach couples two achiral fragments of similar complexity and employs an enantioselective intramolecular Heck reaction to set the absolute stereochemical configuration of an all-carbon quaternary stereocenter. To complete the syntheses of these base- and nucleophile-sensitive natural products, we conduct carefully orchestrated site- and diastereoselective oxidations and other transformations. Our work is the first to generate these targets as single enantiomers.
