76060-35-0 Usage
Uses
Used in Pharmaceutical Industry:
1-Dehydro-6-gingerdione is used as a therapeutic agent for its anti-inflammatory and antioxidant properties, targeting conditions such as cancer, diabetes, and neurodegenerative diseases. Its ability to induce apoptosis and inhibit tumor growth in various cancer cell lines makes it a promising candidate for cancer treatment.
Used in Nutraceutical Industry:
1-Dehydro-6-gingerdione is used as a dietary supplement to enhance overall health and well-being. Its antioxidant and anti-inflammatory properties can help reduce inflammation and oxidative stress, contributing to the prevention and management of chronic diseases.
Used in Cosmetic Industry:
1-Dehydro-6-gingerdione is used as an active ingredient in skincare products for its anti-inflammatory and antioxidant effects. It can help reduce inflammation, promote skin health, and protect against environmental stressors.
Used in Food and Beverage Industry:
1-Dehydro-6-gingerdione is used as a natural preservative and flavor enhancer in food and beverage products. Its antioxidant properties can help extend the shelf life of products, while its anti-inflammatory effects can contribute to the overall health benefits of the products.
Check Digit Verification of cas no
The CAS Registry Mumber 76060-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,6 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76060-35:
(7*7)+(6*6)+(5*0)+(4*6)+(3*0)+(2*3)+(1*5)=120
120 % 10 = 0
So 76060-35-0 is a valid CAS Registry Number.
76060-35-0Relevant academic research and scientific papers
Syntheses of the (+/-)--Gingerols (Pungent Principles of Ginger) and Related Compounds through Regioselective Aldol Condensations: Relative Pungency Assays
Dennif, Phillip,Macleod, Ian,Whiting, Donald A.
, p. 82 - 87 (2007/10/02)
The deprotonation of trimethylsilylzingerone (13) by lithium di-isopropylamide at -78 deg C has been found to be regioselective (92 : 8 in favour of less-substituted enolate): the anion was condensed with alkanals and acyl imidazoles to give convenient syntheses of (+/-)--- and --gingerols (1) and -, -, and -gingerdiones (9).Similary, 3-methoxy-4-trimethylsilyloxybenzylideneacetone (17) gave the (+/-)---dehydrogingerols (8) and -, -, and -dehydrogingerdiones (10).The aldol reaction to -gingerol and methyl -gingerol was also conducted through a vinyloxyborane or through the enol silyl ether (TiCl4 catalysis).Results of organoleptic assays on these compounds are discussed, and the relation between pungency in the gingerols and in capsaicin is commented on.The aldol method was also used to synthesise the natural β-ketols(+/-)-daphneolone (25) and (+/-)-hexahydrocurcumin (4).
