67528-17-0 Usage
Description
2-Dehydrosparteine is a quinolizidine alkaloid that is obtained through formal dehydrogenation at the 2,3-position of sparteine. It is a naturally occurring compound with unique chemical properties and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
2-Dehydrosparteine is used as a pharmaceutical compound for its potential therapeutic effects. Its unique chemical structure allows it to interact with specific biological targets, making it a promising candidate for the development of new drugs.
Used in Chemical Research:
2-Dehydrosparteine is used as a research compound in the field of organic chemistry. Its unique structure and properties make it an interesting subject for studying chemical reactions and mechanisms, as well as for the development of new synthetic methods.
Used in Natural Product Chemistry:
2-Dehydrosparteine is used as a natural product in the study of alkaloids and their biological activities. Its presence in certain plant species provides valuable insights into the biosynthesis of these compounds and their potential applications in medicine and other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 67528-17-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,2 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67528-17:
(7*6)+(6*7)+(5*5)+(4*2)+(3*8)+(2*1)+(1*7)=150
150 % 10 = 0
So 67528-17-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H24N2/c1-3-7-16-11-13-9-12(14(16)5-1)10-17-8-4-2-6-15(13)17/h3,7,12-15H,1-2,4-6,8-11H2/t12-,13-,14+,15-/m0/s1
67528-17-0Relevant articles and documents
2,3-Didehydrosparteine
Ebner, Thomas,Lackner, Helmut,Remberg, Gerd,Meese, Claus O.
, p. 197 - 202 (2007/10/02)
Reduction of lupanine by use of diisobutylaluminium hydride (DIBAH) directly affords (+)-2,3-didehydrosparteine and crystalline (+/-)-3, respectively, in 70percent yield.The conjugate acid of 3 (iminium salt 2) is relatively stable and readily adds cyanide to give 2β-sparteinecarbonitrile (8).On the contrary, enamine 3 undergoes thermal 2->3' dimerisation to give a diastereomeric mixture of 7.The identity of the title compound 3 with the major metabolite of (-)-sparteine (1) has been proven by use of gas chromatography/mass spectrometry.
