6022-36-2 Usage
Uses
Used in Dietary Supplements:
S-equol is used as a dietary supplement for its estrogenic properties, which may help mitigate symptoms of menopause and improve bone health. Its potential health benefits make it a valuable addition to supplements targeting hormonal balance and overall well-being.
Used in Menopause Management:
In the healthcare industry, S-equol is used as a natural alternative to hormone replacement therapy for managing menopause symptoms. Its estrogenic properties can help alleviate hot flashes, night sweats, and other discomforts associated with hormonal changes during menopause.
Used in Bone Health Improvement:
S-equol is used to support bone health due to its potential to improve bone density and reduce the risk of osteoporosis. Its estrogenic effects may contribute to maintaining healthy bone structure and preventing bone loss.
Used in Cancer Prevention:
In the field of oncology, S-equol is being studied for its potential role in reducing the risk of certain hormone-dependent cancers. Its estrogenic properties may help counteract the effects of excess estrogen, which is linked to the development of breast and other hormone-sensitive cancers.
Used in Skincare and Cosmetic Products:
In the cosmetics industry, S-equol is used for its antioxidant and anti-inflammatory properties. It may help protect the skin from oxidative stress and inflammation, promoting a healthier and more youthful appearance. Its potential applications in skincare and cosmetic products make it a valuable ingredient for formulations targeting skin health and rejuvenation.
Check Digit Verification of cas no
The CAS Registry Mumber 6022-36-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,2 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6022-36:
(6*6)+(5*0)+(4*2)+(3*2)+(2*3)+(1*6)=62
62 % 10 = 2
So 6022-36-2 is a valid CAS Registry Number.
6022-36-2Relevant academic research and scientific papers
Synthesis of natural product inulavosin via Ga(OTf)3-Catalyzed Hetero Diels–Alder Dimerization of salicyl alcohol derivative
Gong, Pi-Xian,Li, Hui-Jing,Wang, Meirong,Cheng, Yun-Fei,Wu, Yan-Chao
, p. 2911 - 2916 (2018/10/15)
Inulavosin, a natural melanogenesis inhibitor, has been synthesized smoothly from readily available and inexpensive starting materials by using a Ga(OTf)3-catalyzed room temperature hetero Diels–Alder dimerization of salicyl alcohol derivative and a regioselective phenol monobromination as the key steps.
4,4,4′,4′,7,7′-Hexamethyl-2,2′-spirobichroman
Ejsmont, Krzysztof,Kyziol, Janusz,Nowakowska, Ewa,Zaleski, Jacek
, p. 93 - 94 (2007/10/03)
The title compound, C23H28O2, was obtained from the reaction of acetone with meta-cresol. The molecular structure consists of two identical subunits which are nearly perpendicular to each other. The oxygen-containing rings are not planar and the molecule is chiral. The crystal structure consists of chains of molecules of the same chirality arranged along the [010] axis.
Synthesis of flavans: One-pot synthesis of flavans from 4- methylcoumarins
Kamat, Vijayendra P.,Asolkar, Ratnakar N.,Kirtany, Janardan K.
, p. 4581 - 4587 (2007/10/03)
4-Methylcoumarins (2), obtained by condensation of suitable phenols (1) with ethyl acetoacetate in the presence of sulfuric acid, lead directly to flavans (3) when refluxed with sodium hydroxide and ethanediol.
