517-97-5 Usage
Uses
1. Used in Pharmaceutical Industry:
Tsuduranine is used as a pharmaceutical compound for its potential therapeutic applications. The expression is: "Tsuduranine is used as a pharmaceutical compound for its potential therapeutic applications."
2. Used in Chemical Research:
Tsuduranine is used as a subject of study in chemical research due to its unique properties and the variety of derivatives it can form. The expression is: "Tsuduranine is used as a subject of study in chemical research for its unique properties and the variety of derivatives it can form."
3. Used in Organic Synthesis:
Tsuduranine can be used in organic synthesis to create various compounds and derivatives, contributing to the development of new pharmaceuticals and chemicals. The expression is: "Tsuduranine is used in organic synthesis for the creation of various compounds and derivatives."
References
Goto.,Annalen, 521,175(1935)
Goto, Shishido., ibid, 539,262 (1939)
Goto, Shishido., Proc. Imp. Acad. Tokyo, 15, 8 (1939)
Goto, Yamamato., ibid, 29, 513 (1953)
Check Digit Verification of cas no
The CAS Registry Mumber 517-97-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 517-97:
(5*5)+(4*1)+(3*7)+(2*9)+(1*7)=75
75 % 10 = 5
So 517-97-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H19NO3/c1-21-15-8-11-5-6-19-14-7-10-3-4-12(20)9-13(10)17(16(11)14)18(15)22-2/h3-4,8-9,14,19-20H,5-7H2,1-2H3/t14-/m1/s1
517-97-5Relevant academic research and scientific papers
Guinaudeau, Helene,Freyer, Alan J.,Shamma, Maurice
, p. 1759 - 1764 (1987)
Controlled catalytic hydrogenation of the proaporphine (+)-stepharine (1) proceeded by preferential approach of the catalyst from the side opposite H-6a to provide (+)-8,9-dihydrostepharine (3), accompanied by smaller amounts of (-)-11,12-dihydrostepharine (4) and (+)-tetrahydrostepharine (5).NaBH4 reduction of 5 led to (+)-α- and (+)-β-hexahydrostepharine (6 and 7).Complete spectral and optical data were obtained for all reduction products, thus supplying reliable standards for the characterization of reduced proaporphine alkaloids.
