75656-91-6 Usage
Uses
Used in Pharmaceutical Industry:
Strobamine is used as a pharmaceutical compound for its potential therapeutic applications. Its unique chemical structure and properties make it a promising candidate for the development of new drugs and treatments.
Used in Chemical Research:
Strobamine is used as a research compound in the field of chemistry, particularly in the study of alkaloids and their properties. Its isolation from Knightia strobilina provides valuable insights into the chemical composition and characteristics of this plant species.
Used in Environmental Applications:
Strobamine may also be used in environmental applications, such as in the development of new methods for detecting and monitoring the presence of alkaloids in the environment. Its unique properties could be harnessed to create more efficient and accurate detection techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 75656-91-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,6,5 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75656-91:
(7*7)+(6*5)+(5*6)+(4*5)+(3*6)+(2*9)+(1*1)=166
166 % 10 = 6
So 75656-91-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H19NO2/c1-18-12-7-8-13(18)17-14(19)10-15(20-16(17)9-12)11-5-3-2-4-6-11/h2-6,12-13,15H,7-10H2,1H3/t12-,13+,15-/m0/s1
75656-91-6Relevant academic research and scientific papers
Enantioselective synthesis of strobamine and its analogues
Zhang, Xing,Abraham, Philip,Mascarell, S. Wayne,Flippen-Anderson, Judith,Deschamps, Jeffrey R.,Carrolla, F.Ivy
, p. 96 - 103 (2012/10/30)
(2S,5S,8R)-Strobamine (+)-1a was synthesized by adding cinnamoyl cyanide 6a to tropinone 3 lithium enolate generated by treatment of (S,S')-a,a- dimethyldibenzylamide with butyl lithium in the presence of lithium chloride to give (-)-chalcostrobamine (-)-7a, which yielded a one-to-one mixture of (+)-1a and its C-2 epimer (-)-2a on treatment with 2N sulfuric acid. Compounds (+)-1a and (-)-2a could be separated by column chromatography. (-)-Strobamine (-)-1a and (+)-2a were synthesized by a similar set of reactions using the tropinone 3 lithium enolate generated with butyl lithium in the presence of (R,R')-a,a'-dimethyldibenzylamide and lithium chloride. (+)-and (-)-p-Methylstrobamine (+)-and (-)-1b and (+)-and (-)-epi-p-methylstrobamine (+)-and (-)-2b were synthesized by a similar procedure. The absolute configuration of (+)-epi-pmethylstrobamine (+)-2b was determined by X-ray analysis to have the (2S,5R,8S) configuration. ARKAT USA, Inc.
