60037-43-6 Usage
Description
Acetic acid 4-(2-hydroxyethyl)phenyl ester, also known as 2-(4-Acetoxyphenyl)ethanol, is an organic compound that serves as an intermediate in the synthesis of Oleocanthal (O524540). Acetic acid 4-(2-hydroxyethyl)phenyl ester is derived from olive oil and has been recognized for its potential applications in various fields due to its unique properties.
Uses
Used in Pharmaceutical Industry:
Acetic acid 4-(2-hydroxyethyl)phenyl ester is used as an intermediate for the synthesis of Oleocanthal, a compound with potential applications as an anti-inflammatory and chemotherapeutic agent. Its role in the synthesis process is crucial, as it contributes to the development of pharmaceuticals that can help in managing inflammation and combating cancer.
Used in Olive Oil Research:
In the food industry, specifically in the study of olive oil, Acetic acid 4-(2-hydroxyethyl)phenyl ester plays a significant role. As an intermediate in the synthesis of Oleocanthal, it helps researchers understand the potential health benefits of olive oil and its compounds, which can lead to the development of new products and applications in the food sector.
Used in Cosmetics Industry:
Given its anti-inflammatory properties, Acetic acid 4-(2-hydroxyethyl)phenyl ester can also be used in the cosmetics industry as an ingredient in skincare products. Its potential to alleviate inflammation can make it a valuable component in formulations aimed at reducing skin irritation and promoting a healthy complexion.
Check Digit Verification of cas no
The CAS Registry Mumber 60037-43-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,3 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60037-43:
(7*6)+(6*0)+(5*0)+(4*3)+(3*7)+(2*4)+(1*3)=86
86 % 10 = 6
So 60037-43-6 is a valid CAS Registry Number.
60037-43-6Relevant articles and documents
DIRECT AND MEDIATED EFFECTS ON Bactrocera oleae (GMELIN) (DIPTERA; TEPHRITIDAE) OF NATURAL POLYPHENOLS AND SOME OF RELATED SYNTHETIC COMPOUNDS: STRUCTURE-ACTIVITY RELATIONSHIPS
Capasso, Renato,Evidente, Antonio,Tremblay, Ermenegildo,Sala, Andrea,Santoro, Carmine,et al.
, p. 1189 - 1200 (1994)
Among the main polyphenols occurring in olive oil vegetation waters (VW), catechol showed the most deterrent action on the oviposition of Bactrocera oleae (Gmelin); 4-methylcatechol was less active, whereas hydroxytyrosol and tyrosol were inactive. In con
Regioselective hydrosilylation of epoxides catalysed by nickel(II) hydrido complexes
Wenz, Jan,Wadepohl, Hubert,Gade, Lutz H.
supporting information, p. 4308 - 4311 (2017/04/21)
Bench-stable nickel fluoride complexes bearing NNN pincer ligands have been employed as precursors for the regioselective hydrosilylation of epoxides at room temperature. A nickel hydride assisted epoxide opening is followed by the cleavage of the newly formed nickel oxygen bond by σ-bond metathesis with a silane.
Selective acylation of the phenolic hydroxyl of (hydroxyalkyl)phenols by using vinyl carboxylates as acyl donors in the presence of rubidium fluoride
Miyazawa, Toshifumi,Yamamoto, Masato,Danjo, Hiroshi
, p. 1351 - 1354 (2013/10/01)
Highly selective acylation of the phenolic hydroxy group can be achieved with (hydroxyalkyl)phenols carrying both alcoholic and phenolic hydroxyls by the use of vinyl carboxylates as acyl donors in the presence of rubidium fluoride.
