53492-09-4 Usage
Uses
Used in Pharmaceutical Industry:
(3S,16S)-17α,21-Epoxy-14,15-dihydro-14α-hydroxy-12-methoxyeburnamenine-14-carboxylic acid methyl ester is used as a pharmaceutical compound for its potential therapeutic applications. The specific rotations and ultraviolet spectrum characteristics indicate its unique molecular structure, which may have various biological activities and interactions with biological targets.
Used in Chemical Research:
This alkaloid can be used as a research compound in the field of organic chemistry, particularly for studying its chemical properties, reactivity, and potential applications in the synthesis of other bioactive molecules.
Used in Drug Development:
The unique structural features and biological activities of (3S,16S)-17α,21-Epoxy-14,15-dihydro-14α-hydroxy-12-methoxyeburnamenine-14-carboxylic acid methyl ester may make it a candidate for drug development, particularly in the areas of cancer treatment, neurodegenerative diseases, or other therapeutic areas where its specific properties can be exploited.
Used in Analytical Chemistry:
The specific rotations and ultraviolet spectrum data can be utilized in analytical chemistry for the identification and quantification of this alkaloid in various samples, such as plant extracts or pharmaceutical formulations.
References
Bombardellietal., Tetrahedron, 30, 4141 (1974)
Check Digit Verification of cas no
The CAS Registry Mumber 53492-09-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,9 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53492-09:
(7*5)+(6*3)+(5*4)+(4*9)+(3*2)+(2*0)+(1*9)=124
124 % 10 = 4
So 53492-09-4 is a valid CAS Registry Number.
InChI:InChI=1/C22H26N2O5/c1-27-15-5-3-4-13-14-6-9-23-10-7-16-21(8-11-29-16)12-22(26,20(25)28-2)24(17(13)15)18(14)19(21)23/h3-5,16,19,26H,6-12H2,1-2H3/t16-,19+,21?,22-/m0/s1
53492-09-4Relevant academic research and scientific papers
Stereoselective Synthesis of Indole Alkaloid Cuanzine
Ortuno, J.-C.,Langlois, Y.
, p. 4491 - 4494 (2007/10/02)
Indoliquinolizidines 5 and 6 prepared either by an imino Diels-Alder reaction or by an annulation with Nazarov reagent afforded stereoselectively indole alkaloid cuanzine 1a.Key Words: Cuanzine, indole alkaloid, imino Diels-Alder, Nazarov reagent, methyl isocyanoacetate.
