4684-43-9 Usage
Uses
Used in Pharmaceutical Industry:
Dihydrocorynantheine is used as a medicinal compound for its anti-inflammatory properties, making it a potential candidate for treating inflammatory conditions.
Dihydrocorynantheine is used as an antioxidant agent for its ability to combat oxidative stress, which is implicated in various diseases and aging processes.
Used in Neuroprotective Applications:
In the field of neurology, Dihydrocorynantheine is used as a neuroprotective agent to shield the nervous system from damage, potentially offering benefits in the treatment of neurodegenerative diseases.
Used in Immune System Support:
Dihydrocorynantheine is utilized as an immune system supporter to enhance the body's natural defenses and contribute to overall health.
Used in Arthritis Treatment:
Within the domain of rheumatology, Dihydrocorynantheine is applied as a treatment for arthritis, leveraging its anti-inflammatory effects to alleviate symptoms and improve joint health.
Used in Oncology:
In cancer treatment, Dihydrocorynantheine is used as a potential therapeutic agent, with ongoing research exploring its role in managing or treating malignant conditions.
Used in Neurodegenerative Disease Management:
Dihydrocorynantheine is employed in the management of neurodegenerative diseases, with its neuroprotective qualities under investigation for their potential to slow disease progression or improve patient quality of life.
Check Digit Verification of cas no
The CAS Registry Mumber 4684-43-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,8 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4684-43:
(6*4)+(5*6)+(4*8)+(3*4)+(2*4)+(1*3)=109
109 % 10 = 9
So 4684-43-9 is a valid CAS Registry Number.
4684-43-9Relevant academic research and scientific papers
Total synthesis of (±)-hirsutine: Application of phosphine-catalyzed imine-allene [4 + 2] annulation
Villa, Reymundo A.,Xu, Qihai,Kwon, Ohyun
, p. 4634 - 4637 (2012/10/30)
The total synthesis of the indole alkaloid hirsutine has been achieved, with a key step being the application of our phosphine-catalyzed [4 + 2] annulation of an imine with ethyl α-methylallenoate. From commercially available indole-2-carboxaldehyde, the target was synthesized in 14 steps and 6.7% overall yield.
Preparation of (±)-hirsutine and (±)-3-isocorynantheidine
Lounasmaa, Mauri,Jokela, Reija,Laine, Christiane,Hanhinen, Pirjo
, p. 445 - 450 (2007/10/03)
Preparation of indole alkaloids (±)-hirsutine (1) and (±)-3- isocorynantheidine (2) is described.
Stereoselective Total Synthesis of (+/-)-Hirsutine and Related Corynanthe Alkaloids
Brown, Richard T.,Jones, Martin F.,Wingfield, Mark
, p. 847 - 848 (2007/10/02)
In a completely stereoselective sequence, an analogue of dihydrosecologanin aglucone has been synthesised via a novel cyclopentenedione dimer and converted into tetracyclic indole alkaloids.
