51020-87-2 Usage
Uses
Used in Pharmaceutical Industry:
Licarin B is used as a pharmaceutical agent for its anti-inflammatory, anti-allergic, and anti-cancer properties. It is being researched for its potential to modulate various biological pathways and exert inhibitory effects on tumor growth and progression.
Used in Antioxidant Applications:
Licarin B is used as an antioxidant, which may help protect cells from damage caused by free radicals and oxidative stress. This application is particularly relevant in the context of health and wellness products.
Used in Antifungal Applications:
Licarin B is used as an antifungal agent, potentially offering a natural alternative to synthetic antifungal drugs. This could be beneficial in the development of new treatments for fungal infections.
Used in Anti-Leishmanial Applications:
Licarin B is used as an anti-leishmanial agent, which could be valuable in the treatment of Leishmaniasis, a disease caused by protozoan parasites of the genus Leishmania. This application is significant in the field of tropical medicine and infectious diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 51020-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,0,2 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51020-87:
(7*5)+(6*1)+(5*0)+(4*2)+(3*0)+(2*8)+(1*7)=72
72 % 10 = 2
So 51020-87-2 is a valid CAS Registry Number.
InChI:InChI=1/C20H20O4/c1-4-5-13-8-15-12(2)19(24-20(15)18(9-13)21-3)14-6-7-16-17(10-14)23-11-22-16/h4-10,12,19H,11H2,1-3H3/b5-4+/t12-,19-/m1/s1
51020-87-2Relevant academic research and scientific papers
Synthesis of (±)-licarin B and eupomatenoids-1 and -12: A general approach to 2-aryl-7-alkoxy-benzofuranoid neolignans
Engler, Thomas A.,Chai, Wenying
, p. 6969 - 6970 (2007/10/03)
New synthesis of the title compounds are described using Lewis acid-promoted reactions of styrenes with N-phenylsulfonyl-1,4-benzoquinone monoimines to regioselectively form the 2-arylbenzofuranoid ring system followed by conversion of the aromatic N-phenylsulfonyl moiety into a propenyl substituent.
A regioselective lithiation of ortho-cresols using the bis(dimethylamino)phosphoryl group as a directing group: General synthesis of 2,3-dihydrobenzo[b]furans including naturally occurring neolignans
Watanabe,Kawanishi,Akiyoshi,Furukawa
, p. 3123 - 3131 (2007/10/02)
A general synthetic method was developed for 2-aryl-2,3-dihydrobenzo[b]furans via regioselective lithiation of ortho-tolyl tetramethylphosphorodiamidates followed by addition of aromatic aldehydes as a key step. ortho-Tolyl tetramethylphosphorodiamidates
