850-92-0 Usage
Uses
Used in Pharmaceutical Industry:
2-[2-(3,4-dihydro-6-methoxy-1(2H)-naphthylidene)ethyl]-2-ethylcyclopentane-1,3-dione is used as a potential pharmaceutical agent for its possible antioxidant and anti-inflammatory properties, which may be beneficial in the treatment of various diseases and conditions where oxidative stress and inflammation play a role.
Used in Drug Development:
In the field of drug development, 2-[2-(3,4-dihydro-6-methoxy-1(2H)-naphthylidene)ethyl]-2-ethylcyclopentane-1,3-dione is utilized as a potential enzyme inhibitor or as a structural scaffold for designing new drugs. Its cyclopentane-1,3-dione ring and naphthylidene group may contribute to its interaction with specific biological targets, offering a foundation for the creation of novel therapeutic agents.
Further research is essential to fully understand the properties and potential applications of 2-[2-(3,4-dihydro-6-methoxy-1(2H)-naphthylidene)ethyl]-2-ethylcyclopentane-1,3-dione, as its complex structure suggests a range of possibilities in medicine and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 850-92-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,5 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 850-92:
(5*8)+(4*5)+(3*0)+(2*9)+(1*2)=80
80 % 10 = 0
So 850-92-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H24O3/c1-3-20(18(21)9-10-19(20)22)12-11-14-5-4-6-15-13-16(23-2)7-8-17(14)15/h7-8,11,13H,3-6,9-10,12H2,1-2H3/b14-11-
850-92-0Relevant academic research and scientific papers
A levonorgestrol intermediate preparation method
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Paragraph 0021; 0025; 0027; 0028; 0032; 0034; 0035; 0039, (2018/07/07)
The invention discloses a levonorgestrol intermediate preparation method, in particular relates to a levonorgestrol intermediate format format reagent activity in the reaction control, mainly comprising the reaction is added in the form trichloride or trichloride scandium, stable format reagent activity can be smooth, so that the format reagent and 6 - methoxy - 1 - Tetralone almost without side reaction, reducing the consumption of raw material, yield from the existing technology of 126% increased to 160% left, product HPLC content up to 98% -99.5%.
Catalytic asymmetric torgov cyclization: A concise total synthesis of (+)-estrone
Prevost, Sebastien,Dupre, Nathalie,Leutzsch, Markus,Wang, Qinggang,Wakchaure, Vijay,List, Benjamin
, p. 8770 - 8773 (2014/08/18)
An asymmetric Torgov cyclization, catalyzed by a novel, highly Bronsted acidic dinitro-substituted disulfonimide, is described. The reaction delivers the Torgov diene and various analogues with excellent yields and enantioselectivity. This method was applied in a very short synthesis of (+)-estrone.
