21030-78-4 Usage
Uses
Used in Pharmaceutical Industry:
1,6-Didehydro-3α-methoxy-15,16-[methylenebis(oxy)]-11a-homoerythrinan is used as a potential therapeutic agent for various medical applications due to its unique chemical structure and biological activities. The presence of the methoxyl and methylenedioxy groups may contribute to its pharmacological properties, making it a candidate for further research and development in the pharmaceutical field.
Used in Chemical Research:
1,6-Didehydro-3α-methoxy-15,16-[methylenebis(oxy)]-11a-homoerythrinan is also used as a subject of study in chemical research, particularly in the areas of natural product chemistry, alkaloid chemistry, and structural elucidation. Its unique structure and the presence of specific functional groups make it an interesting target for understanding the relationship between chemical structure and biological activity.
Used in Drug Development:
1,6-Didehydro-3α-methoxy-15,16-[methylenebis(oxy)]-11a-homoerythrinan may be utilized in drug development as a lead compound or as a structural template for the design of new drugs. Its specific rotation and the presence of functional groups could be exploited to optimize its pharmacological properties and target specific biological pathways.
References
Johns et al., Chem. Commun., 1102 (1968)
Check Digit Verification of cas no
The CAS Registry Mumber 21030-78-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,3 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21030-78:
(7*2)+(6*1)+(5*0)+(4*3)+(3*0)+(2*7)+(1*8)=54
54 % 10 = 4
So 21030-78-4 is a valid CAS Registry Number.
21030-78-4Relevant academic research and scientific papers
Total synthesis of homoerythrinan alkaloids, schelhammericine and 3-epischelhammericine
Tsuda, Yoshisuke,Ohshima, Takeshi,Hosoi, Shinzo,Kaneuchi, Satomi,Kiuchi, Fumiyuki,Toda, Jun,Sano, Takehiro
, p. 500 - 508 (2007/10/03)
Total syntheses of two homoerythrinan alkaloids, schelhammericine and 3-epischelhammericine, are described. Photocycloaddition of a dioxopyrrolobenzazepine to 1-methoxy-3-trimethylsilyloxybutadiene afforded, in a regio- and stereo-specific manner, the cyc
Total synthesis of the homoerythrinan alkaloids, schelhammericine and 3-epischelhammericine
Tsuda,Hosoi,Ohshima,et al.
, p. 3574 - 3577 (2007/10/02)
This stereo-coantrolled total synthesis of the title alkaloids, both in racemic form, is the first synthesis of the naturally occurring homoerythrinan alkaloids.
