133601-13-5 Usage
Description
1(2H)-Naphthalenone, 3,4-dihydro-8-(hydroxymethyl)-, also known as Hederagenin, is a chemical compound with the molecular formula C11H12O3. It is a white crystalline powder that is primarily used in the pharmaceutical and cosmetic industries. Hederagenin is a triterpenoid saponin that is commonly found in several plants, including ivy and ginseng. It has been studied for its potential medicinal properties, including anti-inflammatory, anti-cancer, and anti-diabetic effects. Additionally, Hederagenin has been investigated for its ability to enhance skin health and improve wound healing, making it a valuable ingredient in skincare products. Overall, Hederagenin is a versatile compound with various potential applications in the fields of medicine and cosmetics.
Uses
Used in Pharmaceutical Industry:
1(2H)-Naphthalenone, 3,4-dihydro-8-(hydroxymethyl)is used as a medicinal compound for its potential anti-inflammatory, anti-cancer, and anti-diabetic effects. Its presence in various plants and its ability to modulate several signaling pathways make it a promising candidate for the development of new drugs and therapies.
Used in Cosmetic Industry:
1(2H)-Naphthalenone, 3,4-dihydro-8-(hydroxymethyl)is used as an ingredient in skincare products for its ability to enhance skin health and improve wound healing. Its beneficial properties contribute to the development of effective cosmetic formulations that promote skin regeneration and overall skin wellness.
Check Digit Verification of cas no
The CAS Registry Mumber 133601-13-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,6,0 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 133601-13:
(8*1)+(7*3)+(6*3)+(5*6)+(4*0)+(3*1)+(2*1)+(1*3)=85
85 % 10 = 5
So 133601-13-5 is a valid CAS Registry Number.
133601-13-5Relevant articles and documents
Photocyclization Reactions. Part 3 [1]. Synthesis of Naphtho[1,8-bc]-furans and Cyclohepta[cd]benzofurans Using Photocyclization of 8-Alkoxy-1,2,3,4-tetrahydro-1-naphthalenones and 4-Alkoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ones
Sharshira, Essam Mohamed,Iwanami, Haruki,Okamura, Mutsuo,Hasegawa, Eietsu,Horaguchi, Takaaki
, p. 17 - 25 (2007/10/03)
Photocyclization reactions were carried out on 8-alkoxy-1,2,3,4-tetrahydro-1-naphthalenones (six-membered ring ketones) 4a-g and 4-alkoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ones (seven-membered ring ketones) 5a-e in acetonitrile. Irradiation of 4a-f gave rearranged naphthyl alcohols 8a-f as major products. In the case of 4g, 2a,3,4,5-tetrahydronaphtho[1,8-bc]furan-2a-ol 6g was obtained. In contrast, irradiation of 5a-e afforded 2,2a,3,4,5,6-hexahydrocyclohepta[cd]benzofuran-2a-ols 9a-e in good yields. The difference in reactivities between 4a-g and 5a-e is attributed to the conformation of six- and seven-membered rings. Conformational and substituent effects in cyclization step of 1,5-biradicals are discussed along with reaction pathways.
