529-79-3 Usage
General Description
(5S,11S)-5,6,11,12-Tetrahydro-2,3,8,9-tetramethoxy-5,11-epiminodibenzo[a,e]cyclooctene is a complex, multi-substituted compound with four methoxy groups and an epimino functionality. It belongs to the dibenzo[a,e]cyclooctene family and has a cyclooctene core structure. This chemical is classified as a cycloalkene and contains nitrogen, oxygen, and carbon atoms. It is a chiral compound with two stereocenters at positions 5 and 11. The unique structure and substitution pattern of this compound make it a potentially interesting molecule for pharmaceutical or chemical research, offering opportunities for further exploration in areas such as drug discovery or synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 529-79-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 529-79:
(5*5)+(4*2)+(3*9)+(2*7)+(1*9)=83
83 % 10 = 3
So 529-79-3 is a valid CAS Registry Number.
529-79-3Relevant articles and documents
An Enantioselective Access to 1-Alkyl-1,2,3,4-tetrahydroisoquinolines. Application to a New Synthesis of (-)-Argemonine
Youte, Jean-Jacques,Barbier, Denis,Al-Mourabit, Ali,Gnecco, Dino,Marazano, Christian
, p. 2737 - 2740 (2007/10/03)
Potassium ferricyanide oxidation of salt 1 gave isoquinolinone 7 whose treatment with Grignard reagents resulted in a high-yield formation of substituted isoquinolinium salts 5. The selectivity of the reduction of these salts to give derivatives 6 has been studied. Particularly good selectivities (82-84%) were observed when R is a benzylic group. On the basis of these results, a practical and enantioselective synthesis of the natural alkaloid (-)-argemonine is presented.
