6882-72-0 Usage
Uses
1-Acetylaspidospermidine-3α,17-diol has potential applications in various industries, including pharmaceutical, chemical, and research sectors. Some of its uses are as follows:
Used in Pharmaceutical Industry:
1-Acetylaspidospermidine-3α,17-diol is used as a pharmaceutical compound for its potential therapeutic properties. Its unique structure and functional groups may contribute to the development of new drugs or drug candidates for the treatment of various diseases.
Used in Chemical Research:
1-Acetylaspidospermidine-3α,17-diol is used as a research chemical for studying its chemical properties, reactivity, and potential applications in the synthesis of other compounds. Its unique structure and functional groups make it an interesting subject for chemical investigations.
Used in Natural Product Chemistry:
1-Acetylaspidospermidine-3α,17-diol is used as a natural product for studying its occurrence, distribution, and potential biological activities. Its isolation from the bark of Aspidosperma chakense Spagazzini highlights the importance of exploring natural sources for novel and bioactive compounds.
References
Djerassi et a!., Experientia, 18, 113 (1962)
Djerassi et al., 1. Amer. Chem. Soc., 84, 3480 (1962)
Check Digit Verification of cas no
The CAS Registry Mumber 6882-72-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,8 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6882-72:
(6*6)+(5*8)+(4*8)+(3*2)+(2*7)+(1*2)=130
130 % 10 = 0
So 6882-72-0 is a valid CAS Registry Number.
InChI:InChI=1/C21H28N2O3/c1-3-20-8-5-10-22-11-9-21(19(20)22)14-6-4-7-15(25)17(14)23(13(2)24)18(21)16(26)12-20/h4,6-7,16,18-19,25-26H,3,5,8-12H2,1-2H3/t16-,18+,19+,20+,21+/m0/s1
6882-72-0Relevant academic research and scientific papers
Divergent total syntheses of (-)-aspidospermine and (+)-spegazzinine
Lajiness, James P.,Jiang, Wanlong,Boger, Dale L.
, p. 2078 - 2081 (2012/06/18)
Divergent total syntheses of (+)-spegazzinine (1) and (-)-aspidospermine (2) and their extensions to the synthesis of C19-epi-aspidospermine and C3-epi-spegazzinine are detailed, confirming the relative stereochemistry and establishing the absolute configuration of (+)-spegazzinine. A powerful intramolecular [4 + 2]/[3 + 2] cycloaddition cascade of a 1,3,4-oxadiazole provided the pentacyclic skeleton and all the requisite stereochemistry of the natural products in a single reaction that forms three rings, four C-C bonds, and five stereocenters.
