36752-54-2 Usage
Uses
Used in Pharmaceutical Applications:
10-Shogaol is used as a therapeutic agent for its antioxidant activity, which can help combat oxidative stress and related health issues. Its hypolipidemic effects make it a potential candidate for managing dyslipidemia, while its insulin-sensitizing properties suggest a role in diabetes management.
Used in Nutraceutical Applications:
In the nutraceutical industry, 10-Shogaol is used as a supplement ingredient to promote overall health and well-being. Its antioxidant properties can contribute to a stronger immune system and cellular protection, while its hypolipidemic and insulin-sensitizing effects may support cardiovascular and metabolic health.
Used in Cosmetic Applications:
10-Shogaol is used as an active ingredient in the cosmetic industry for its antioxidant and anti-inflammatory properties. It can be incorporated into skincare products to help protect the skin from environmental stressors, reduce inflammation, and promote a healthier, more radiant complexion.
Used in Functional Food and Beverage Applications:
10-Shogaol can be used as an additive in the functional food and beverage industry to enhance the health benefits of these products. Its antioxidant, hypolipidemic, and insulin-sensitizing effects can provide consumers with additional health advantages when incorporated into their diets.
Check Digit Verification of cas no
The CAS Registry Mumber 36752-54-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,5 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 36752-54:
(7*3)+(6*6)+(5*7)+(4*5)+(3*2)+(2*5)+(1*4)=132
132 % 10 = 2
So 36752-54-2 is a valid CAS Registry Number.
InChI:InChI=1/C21H32O3/c1-3-4-5-6-7-8-9-10-11-12-19(22)15-13-18-14-16-20(23)21(17-18)24-2/h11-12,14,16-17,23H,3-10,13,15H2,1-2H3/b12-11+
36752-54-2Relevant academic research and scientific papers
Kinetic Resolution of β-Hydroxy Carbonyl Compounds via Enantioselective Dehydration Using a Cation-Binding Catalyst: Facile Access to Enantiopure Chiral Aldols
Paladhi, Sushovan,Hwang, In-Soo,Yoo, Eun Jeong,Ryu, Do Hyun,Song, Choong Eui
supporting information, p. 2003 - 2006 (2018/04/16)
A practical and highly enantioselective nonenzymatic kinetic resolution of racemic β-hydroxy carbonyl (aldol) compounds through enantioselective dehydration process was developed using a cation-binding Song's oligoethylene glycol (oligoEG) catalyst with p
