77757-14-3 Usage
Alkaloid
13,15-dideoxyaconitine is an alkaloid, which is a type of naturally occurring organic compound that contains mostly basic nitrogen atoms.
Toxicity
13,15-dideoxyaconitine is a toxic compound that can cause severe health problems, including numbness, tingling, paralysis, and respiratory failure.
Neurotoxin
13,15-dideoxyaconitine is a potent neurotoxin that affects the central nervous system.
Structural similarity
13,15-dideoxyaconitine is structurally similar to aconitine, another toxic alkaloid found in aconite plants.
Potential for poisoning
Due to its toxicity, 13,15-dideoxyaconitine has the potential to cause poisoning, which is a significant concern.
Chemical weapon
13,15-dideoxyaconitine has been studied for its potential use as a chemical weapon due to its high toxicity.
Medicinal use
13,15-dideoxyaconitine is used in traditional Chinese medicine for its analgesic properties, but its use is highly regulated and controlled.
Plant source
13,15-dideoxyaconitine is found in the Aconitum species of plants, commonly known as aconite or monkshood.
Check Digit Verification of cas no
The CAS Registry Mumber 77757-14-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,7,5 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 77757-14:
(7*7)+(6*7)+(5*7)+(4*5)+(3*7)+(2*1)+(1*4)=173
173 % 10 = 3
So 77757-14-3 is a valid CAS Registry Number.
InChI:InChI=1/C34H47NO8/c1-7-35-17-32(18-38-3)14-13-24(40-5)34-22-15-21-23(39-4)16-33(43-19(2)36,26(30(34)35)28(41-6)29(32)34)25(22)27(21)42-31(37)20-11-9-8-10-12-20/h8-12,21-30H,7,13-18H2,1-6H3
77757-14-3Relevant academic research and scientific papers
STRUCTURE OF EZOCHASMANINE, EZOCHASMACONITINE, ANISOEZOCHASMACONITINE AND SYNTHESIS OF VILMORRIANINE A
Takayama, Hiromitsu,Ito, Miyuki,Koga, Miyuki,Sakai, Shin-ichiro,Okamoto, Toshihiko
, p. 403 - 408 (2007/10/02)
The structures of new diterpene alkaloids, ezochasmanine, ezochasmaconitine, and anisoezochasmaconitine, have been established as 3-hydroxychasmanine, 14-acetyl-8-benzoylchasmanine, and 14-acetyl-8-anisoylchasmanine respectively, in correlation with a known alkaloid chasmanine.Vilmorrianine A (8-acetyl-14-anisoylezochasmanine) was synthesized from ezochasmanine via benzoylation, trichloroethoxycarbonylation, acetylation and elimination reaction of trichloroethoxycarbonyl group.
