143615-75-2 Usage
Uses
Used in Natural Medication and Supplements:
Diacetoxy-6-gingerdiol is used as a potential health-promoting compound for its antioxidant, anti-inflammatory, and anti-cancer properties. It is found in the ginger plant and is part of the gingerols group, which contributes to ginger's unique flavor and health benefits.
Used in Antioxidant Applications:
Diacetoxy-6-gingerdiol is used as an antioxidant, helping to protect cells from damage caused by free radicals and oxidative stress. Its antioxidant properties may contribute to the overall health benefits associated with ginger consumption.
Used in Anti-inflammatory Applications:
Diacetoxy-6-gingerdiol is used as an anti-inflammatory agent, potentially reducing inflammation and pain in the body. Its anti-inflammatory effects may be beneficial for individuals suffering from various inflammatory conditions.
Used in Anti-cancer Applications:
Diacetoxy-6-gingerdiol is used as a potential anti-cancer agent, with studies suggesting it may have the ability to inhibit cancer cell growth and proliferation. Further research is needed to fully understand its mechanisms and potential applications in cancer treatment.
Check Digit Verification of cas no
The CAS Registry Mumber 143615-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,6,1 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 143615-75:
(8*1)+(7*4)+(6*3)+(5*6)+(4*1)+(3*5)+(2*7)+(1*5)=122
122 % 10 = 2
So 143615-75-2 is a valid CAS Registry Number.
143615-75-2Relevant academic research and scientific papers
GINGEROL COMPOUNDS AND THEIR USE AS FLAVOR MODIFIERS
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Page/Page column 58; 59, (2021/05/21)
The present disclosure relates to gingerol compounds, whether in their diol form or as a derivative, and their use to enhance the salty taste or the umami taste of a flavored article. The disclosure also provides compositions and flavored products contain
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.
