717-47-5 Usage
Derivation
2-(1,1-Dimethylethyl)-1,4-benzenediol 4-acetate is derived from the dihydroxybenzene family.
Common uses
It is commonly used as an antioxidant in various industries, including pharmaceuticals, food, and personal care products.
Anti-inflammatory and anti-cancer properties
2-(1,1-Dimethylethyl)-1,4-benzenediol 4-acetate is known for its potential anti-inflammatory and anti-cancer properties.
Anti-aging ingredient
It is often added to cosmetic and skincare products as an anti-aging ingredient due to its ability to protect against oxidative stress and environmental damage.
Treatment of inflammatory skin conditions
2-(1,1-Dimethylethyl)-1,4-benzenediol 4-acetate has shown promise in the treatment of certain inflammatory skin conditions.
Potential as a therapeutic agent in cancer treatment
It has been researched for its potential as a therapeutic agent in cancer treatment.
Check Digit Verification of cas no
The CAS Registry Mumber 717-47-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 717-47:
(5*7)+(4*1)+(3*7)+(2*4)+(1*7)=75
75 % 10 = 5
So 717-47-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H16O3/c1-8(13)15-9-5-6-11(14)10(7-9)12(2,3)4/h5-7,14H,1-4H3
717-47-5Relevant academic research and scientific papers
Utilization of the inherent nucleophile for regioselective O-acylation of polyphenols via an intermolecular cooperative transesterification
Liu, Jingchao,Fu, Junjie,Li, Wenlong,Zou, Yu,Huang, Zhangjian,Xu, Jinyi,Peng, Sixun,Zhang, Yihua
, p. 4103 - 4110 (2016/07/06)
A green and efficient method for regioselective O-acylation of polyphenols has been developed. The acylation can be carried out in potassium carbonate/dimethyl sulphoxide system by utilizing the ‘inherent nucleophile’ via an intermolecular cooperative transesterification under mild condition. This method shows particular advantage in regioselective acylation of polyphenols bearing 2′,4′-dihydroxyacetophenone moiety and can be extended to the synthesis of mono or multiple acetates of polyphenols without this moiety in good yields. Compared with other reported approaches, this method is endowed with atom economy and is more environment-friendly for avoiding the use of any metal-based catalysts.
New polymer-supported phosphonate reagents for the synthesis of Z-α,β-unsaturated esters
Ando, Kaori,Suzuki, Yusaku
scheme or table, p. 2323 - 2325 (2010/06/13)
New polymer-supported phosphonate reagents have been prepared and evaluated for the synthesis of Z-α,β-unsaturated esters. High Z-selectivity was obtained using the reagent having two o-t-BuC6H4 groups.
