160436-10-2 Usage
Uses
Used in Pharmaceutical Industry:
3',5,5',7-Tetrahydroxyflavane is used as a pharmaceutical agent for its potential to prevent oxidative stress and inflammation, which could potentially benefit conditions such as neurodegenerative diseases, cancer, and cardiovascular disease.
Used in Nutritional Supplements:
3',5,5',7-Tetrahydroxyflavane is used as a nutritional supplement for its antioxidant properties, which contribute to potential health benefits and support overall well-being.
Used in Cosmetics Industry:
3',5,5',7-Tetrahydroxyflavane is used as an ingredient in cosmetics for its potential anti-aging and skin health benefits due to its antioxidant and anti-inflammatory properties.
Used in Functional Foods:
3',5,5',7-Tetrahydroxyflavane is used as an additive in functional foods for its potential health-promoting effects, including neuroprotection and support for cardiovascular health.
Check Digit Verification of cas no
The CAS Registry Mumber 160436-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,4,3 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 160436-10:
(8*1)+(7*6)+(6*0)+(5*4)+(4*3)+(3*6)+(2*1)+(1*0)=102
102 % 10 = 2
So 160436-10-2 is a valid CAS Registry Number.
160436-10-2Relevant academic research and scientific papers
Huazhongilexone is not 3′,5,5′,7-tetrahydroxyflavanone. Preparation of 3′,5′-dimethoxy-5,7-dihydroxyflavanone
Anthoni, Uffe,Encarnacion D., Rosalba,Nielsen, Per H.,Christophersen, Garsten
, p. 1243 - 1246 (2007/10/03)
Huazhongilexone, isolated from Ilex centrochinensis, was originally assigned the structure 3′,5,5′,7-tetrahydroxyflavanone. The racemic flavanone has been synthezised. Huazhongilexone is different from the synthetic compound and thus must have a different structure. In addition the new (±)-3′,5′-dimethoxy-5,7- dihydroxyflavanone has been prepared and characterized. Acta Chemica Scandinavica 1998.
One step synthesis of polyhydroxyflavan ones from hydroxyacetophenones and hydroxybenzaldehydes
Chan, Wing Lai,Lin, Yong Cheng,Zhang, Wei Han,Tang, Pak Lai,Szeto, Yau Shan
, p. 551 - 554 (2007/10/03)
Polyhydroxyflavanones were synthesized in a one-step process by reacting the appropriate hydroxyacetophenones and hydroxybenzaldehydes in the presence of boric acid, in a mixed solvent system.
