2752-64-9 Usage
Uses
Used in Pharmaceutical Industry:
Mesaconitine is used as a pharmaceutical compound for its potential therapeutic effects. Its alkaloid nature allows it to interact with specific receptors in the body, making it a candidate for the development of new drugs targeting various medical conditions.
Used in Traditional Medicine:
Mesaconitine has been utilized in traditional medicine, particularly in Chinese medicine, for its analgesic and anti-inflammatory properties. It is used to alleviate pain and reduce inflammation in various conditions.
Used in Research and Development:
Due to its unique chemical structure and properties, Mesaconitine is used as a research compound for studying the effects of aconitine alkaloids on biological systems. This helps in understanding their mechanisms of action and potential applications in medicine.
Used in Toxicology Studies:
Mesaconitine is also used in toxicology studies to understand the effects of aconitine alkaloids on the human body. This knowledge is crucial for developing safety guidelines and antidotes for potential poisoning incidents.
References
Jacobs, Pelletier, Chern. & Ind., 591 (1960)
Furner, Jeschka, Gibson,J. Arner. Chern. Soc., 82,5182 (1960)
Check Digit Verification of cas no
The CAS Registry Mumber 2752-64-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,5 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2752-64:
(6*2)+(5*7)+(4*5)+(3*2)+(2*6)+(1*4)=89
89 % 10 = 9
So 2752-64-9 is a valid CAS Registry Number.
InChI:InChI=1/C33H45NO11/c1-16(35)45-33-21-18(13-31(39,28(43-6)26(33)37)27(21)44-29(38)17-10-8-7-9-11-17)32-20(41-4)12-19(36)30(15-40-3)14-34(2)25(32)22(33)23(42-5)24(30)32/h7-11,18-28,36-37,39H,12-15H2,1-6H3/t18-,19-,20+,21-,22+,23+,24-,25?,26+,27-,28+,30+,31-,32+,33-/m1/s1
2752-64-9Relevant articles and documents
DEOXYGENATION REACTIONS OF C19-DITERPENOID ALKALOIDS
Kulanthaivel, Palaniappan,Pelletier, S. William
, p. 4313 - 4320 (2007/10/02)
Efficient methods for deoxygenation of secondary and tertiary alcohols of some C19-diterpenoid alkaloids are presented.Delphisine (12) was converted to 1-deoxydelphisine (19) via either 1,2-pyrodelphisine (17) or phenyl thionocarbonate 20.The following alkaloids were deoxygenated via their thiocarbonylimidazolyl derivatives: 14-acetyldelcosine (13) to 14-acetyl-1-deoxydelcosine (22); alkaline hydrolysis of 22 gave 1-deoxydelcosine (23); aconitine (24) to 3-deoxyaconitine (27); yunaconitine (25) to crassicauline A (28).Deoxygenation of 14-acetyldictyocarpine (30) via the chloro-derivate 31 gave 14-acetyl-10-deoxydictiocarpine (34).Reduction of 31 with LiAlH4 gave the unusual elimination product 32.An improved partial synthesis of hypaconitine (35) from aconitine (24) is also presented.