5096-71-9 Usage
Uses
Thalicberine methyl ether has various applications in different industries, including:
Used in Pharmaceutical Industry:
Thalicberine methyl ether is used as a pharmaceutical compound for its potential therapeutic properties. It has been studied for its potential effects on the central nervous system, as well as its potential use in the treatment of various diseases and conditions.
Used in Chemical Research:
Thalicberine methyl ether is also used as a research compound in the field of organic chemistry. Its unique structure and properties make it a valuable tool for studying the synthesis and reactions of alkaloids and other related compounds.
Used in Traditional Medicine:
Thalicberine methyl ether has been used in traditional medicine for centuries, particularly in East Asia. It is believed to have various health benefits and is used to treat a range of ailments, including digestive disorders, respiratory issues, and skin conditions.
References
Yunusov, Progressov., J. Gen. Chem., USSR, 20, 1151 (1950)
Check Digit Verification of cas no
The CAS Registry Mumber 5096-71-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,9 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5096-71:
(6*5)+(5*0)+(4*9)+(3*6)+(2*7)+(1*1)=99
99 % 10 = 9
So 5096-71-9 is a valid CAS Registry Number.
InChI:InChI=1/C38H42N2O6/c1-39-15-13-25-20-34-32(42-4)22-28(25)29(39)17-23-7-10-27(11-8-23)45-33-19-24(9-12-31(33)41-3)18-30-36-26(14-16-40(30)2)21-35(43-5)37(44-6)38(36)46-34/h7-12,19-22,29-30H,13-18H2,1-6H3/t29-,30-/m0/s1
5096-71-9Relevant academic research and scientific papers
ENZYMIC CONTROL OF STEREOCHEMISTRY AMONG THE THALICTRUM BISBENZYLISOQUINOLINE ALKALOIDS
Guinaudeau, Helene,Freyer, Alan J.,Shamma, Maurice,Baser, Kemal Husnu Can
, p. 1975 - 1982 (2007/10/02)
The new bisbenzylisoquinolines (+)-thaligrisine and (+)-thaliphylline 6 have been isolated from Thalictrum minus var. microphyllum.Four rules are described which correlate the structures os Thalictrum bisbenzylisoquinolines with their stereochemistry at C-1 and C-1'.As a result, (+)-thalrugosamine is shown to be identical with (+)-homoaromoline 14. (+)-Thalisamine and (+)-N'-norhernandezine are also identical and are represented by expression 18.The sole exception to the rules is (-)-isothalidezine 15.