916264-22-7 Usage
Description
Acetylvirolin is a chemical compound that belongs to the class of acetylated virolins, which are naturally occurring compounds found in certain plants. It possesses potential anti-inflammatory and antifungal properties, making it a subject of research for pharmaceutical and medical applications.
Uses
Used in Pharmaceutical Industry:
Acetylvirolin is used as an anti-inflammatory agent for its potential to reduce inflammation and alleviate symptoms associated with inflammatory conditions.
Used in Antifungal Applications:
Acetylvirolin is used as an antifungal agent for its ability to inhibit the growth of fungal pathogens, offering a potential treatment for various fungal infections.
Further research and clinical trials are needed to fully understand the therapeutic potential and safety profile of acetylvirolin for use in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 916264-22-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,2,6 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 916264-22:
(8*9)+(7*1)+(6*6)+(5*2)+(4*6)+(3*4)+(2*2)+(1*2)=167
167 % 10 = 7
So 916264-22-7 is a valid CAS Registry Number.
916264-22-7Relevant articles and documents
Streamlined, asymmetric synthesis of 8,4′-oxyneolignans
Curti, Claudio,Zanardi, Franca,Battistini, Lucia,Sartori, Andrea,Rassu, Gloria,Pinna, Luigi,Casiraghi, Giovanni
, p. 8552 - 8558 (2007/10/03)
Highly direct, modular syntheses of several natural 8,4′- oxyneolignans [(-)-1, (+)-1, (-)-2, and (-)-3] and some related variants [(-)-26, (+)-26, (+)-27, and (-)-28] are reported. Utilizing (S)- or (R)-methyl lactate as the chiral sources, two complementary syn- or anti-oriented routes were designed, encompassing nine and five steps, which were carried out to deliver the targets in an enantiomerically pure form. The embodiment of the two independent aryl and aryloxy moieties onto the lactate frame was performed according to a diversity-oriented protocol from the common precursors, aldehydes 6 and ent-6 for the syn-oriented routes and mesyl esters 19 and ent-19 for the anti-oriented routes. These syntheses set the stage for the generation of a wide and diverse repertoire of 8,4′-oxyneolignan compounds and the broad biological interrogation of its members.
