863780-90-9 Usage
Description
Methyl diacetoxy-6-gingerdiol is a chemical compound derived from ginger, specifically from the diol component of its essential oil. It is known for its anti-inflammatory and antioxidant properties, which make it a popular ingredient in natural health and wellness products. Its acetoxy groups enable it to effectively modulate various signaling pathways related to inflammatory processes, making it a potential candidate for the development of new pharmaceuticals for the treatment of inflammatory conditions. Additionally, studies have shown that this compound has potential as a therapeutic agent for neurodegenerative diseases, further highlighting its versatility and potential in the field of medicine and health.
Uses
Used in Natural Health and Wellness Products:
Methyl diacetoxy-6-gingerdiol is used as an ingredient in natural health and wellness products for its anti-inflammatory and antioxidant properties.
Used in Pharmaceutical Development:
Methyl diacetoxy-6-gingerdiol is used as a potential candidate for the development of new pharmaceuticals for the treatment of inflammatory conditions due to its ability to modulate various signaling pathways related to inflammatory processes.
Used in Neurodegenerative Disease Treatment:
Methyl diacetoxy-6-gingerdiol is used as a therapeutic agent for neurodegenerative diseases, as studies have shown its potential in this area.
Check Digit Verification of cas no
The CAS Registry Mumber 863780-90-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,7,8 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 863780-90:
(8*8)+(7*6)+(6*3)+(5*7)+(4*8)+(3*0)+(2*9)+(1*0)=209
209 % 10 = 9
So 863780-90-9 is a valid CAS Registry Number.
863780-90-9Relevant articles and documents
Synthesis of gingerol and diarylheptanoids
Sabitha, Gowravaram,Srinivas, Chitti,Reddy, Teega Rammohan,Yadagiri, Kurra,Yadav, Jhillu Singh
, p. 2124 - 2133 (2012/03/27)
The synthesis of gingerol 1 and related compounds 2-5 along with diarylheptanoids 6-8 has been accomplished using a Keck allylation, Crimmins' aldol reaction, aldehyde coupling with acetylene, and chelation controlled reductions as the key reactions. The absolute configuration of these molecules was confirmed by preparing their acetonide derivatives and by comparison of the NMR data with natural compounds.
