6565-70-4 Usage
Uses
Used in Personal Care Industry:
4-Octylbenzene-1,3-diol is used as an ingredient in personal care products for its antioxidant and anti-inflammatory properties, making it suitable for sunscreens and skincare products.
Used in Plastics and Rubber Industry:
4-Octylbenzene-1,3-diol is used as a component in the production of UV absorbers and stabilizers for plastics and rubber products, enhancing their durability and resistance to UV degradation.
Used in Pharmaceutical Industry:
4-Octylbenzene-1,3-diol has potential applications in medicine and pharmaceuticals due to its biological activities, including potential anti-cancer and antimicrobial properties. However, further studies are required to fully understand and harness the potential benefits of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 6565-70-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,6 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6565-70:
(6*6)+(5*5)+(4*6)+(3*5)+(2*7)+(1*0)=114
114 % 10 = 4
So 6565-70-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H22O2/c1-2-3-4-5-6-7-8-12-9-10-13(15)11-14(12)16/h9-11,15-16H,2-8H2,1H3
6565-70-4Relevant academic research and scientific papers
Antifungal Activity of 2,4-Dihydroxyacylophenones and Related Compounds
Mizobuchi, Shigeyuki,Sato, Yuko
, p. 1327 - 1334 (2007/10/02)
The antifungal activity of 2,4-dihydroxyacylophenones and related compounds against Trichophyton spp. and other fungi were investigated to determine their structure-activity relationships.The activity of these compounds was found to be closely related to the length of the acyl and alkyl substituents attached to the 1,3-dihydroxybenzene moiety.In addition, differences in activity were observed depending on the position of the alkyl substituents and on the number of substituents attached to the 1,3-dihydroxybenzene moiety.Some compounds tested showed potent antifungal activity against Trichophyton spp. and other fungi that was more active than amphotericin B.
N-alkylated cresylic acids via direct alkylation in a liquid phase
-
, (2008/06/13)
A method for the production of n-alkylated cresylic acids such as n-hexyl resorcinol by direct alkylation of a cresylic acid such as resorcinol under liquid phase conditions.
