72785-25-2 Usage
Molecular Structure
The chemical 2-(4-methoxybenzyloxyphenyl)-ethyl-N-methylamine consists of a benzyl ether group, a phenyl ring, an ethyl chain, and an N-methylamine group.
Usage
It is primarily used in medicinal chemistry as a building block for the synthesis of various biologically active compounds, including pharmaceutical drugs.
Therapeutic Applications
The compound can be utilized in the development of new drug candidates for the treatment of various diseases, such as cancer, neurological disorders, and cardiovascular conditions.
Structural Features
Its structural features make it a valuable tool in the discovery and development of novel therapeutic agents.
Versatility
Its versatility and potential for modification make it a valuable asset in drug discovery and development research.
Check Digit Verification of cas no
The CAS Registry Mumber 72785-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,8 and 5 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72785-25:
(7*7)+(6*2)+(5*7)+(4*8)+(3*5)+(2*2)+(1*5)=152
152 % 10 = 2
So 72785-25-2 is a valid CAS Registry Number.
72785-25-2Relevant articles and documents
SYNTHESIS OF GALANTHAMINE AND RELATED ALKALOIDS - NEW APPROARCHES. I.
Vlahov, Radoslav,Krikorian, Dikran,Spassov, Grigor,Chinova, Maja,Vlahov, Ioncho,et al.
, p. 3329 - 3346 (2007/10/02)
Modifications of protecting groups and of the oxidative coupling conditions led to pure crystalline intermediates in the synthesis of galanthamine derivatives and gave dienone A in better yields than reported before.The E-configuration of amide 3' in crystalline state has been determined by X-ray diffraction.Streptomyces affinis 6737 reduces A to the optically active (-)-epigalanthamine derivative C, whose absolute configuration was determined by Bijvoet's method.Nematospora corylii CBS 2608 reduces to racemic B.With Ashbya gossypii IFO 1355 a mixture of racemic B and of optically active C is obtained.Some other microbial transformations are described.
