72712-21-1 Usage
Description
ACETIC ACID 2-ACETOXY-5-ACETYL-PHENYL ESTER is a chemical compound with the molecular formula C11H12O4, derived from the esterification of acetic acid and 2-acetoxy-5-acetylphenol. It is a versatile intermediate in the synthesis of various pharmaceuticals, perfumes, and flavoring agents, and has been studied for its potential anti-inflammatory and antioxidant properties.
Uses
Used in Pharmaceutical Industry:
ACETIC ACID 2-ACETOXY-5-ACETYL-PHENYL ESTER is used as an intermediate in the synthesis of various drugs, contributing to the development of new medications with diverse therapeutic applications.
Used in Cosmetic Industry:
In the cosmetic industry, ACETIC ACID 2-ACETOXY-5-ACETYL-PHENYL ESTER serves as an intermediate in the production of perfumes, enhancing the fragrance profiles of various cosmetic products.
Used in Food Industry:
ACETIC ACID 2-ACETOXY-5-ACETYL-PHENYL ESTER is utilized as a flavoring agent, imparting unique taste and aroma characteristics to food products, thereby enriching the sensory experience of consumers.
Used in Research and Development:
ACETIC ACID 2-ACETOXY-5-ACETYL-PHENYL ESTER is also used in research settings to explore its potential biological activities, such as anti-inflammatory and antioxidant properties, which could lead to the discovery of new therapeutic agents or health supplements.
It is crucial to handle ACETIC ACID 2-ACETOXY-5-ACETYL-PHENYL ESTER with care, ensuring proper use and storage to avoid any hazardous effects.
Check Digit Verification of cas no
The CAS Registry Mumber 72712-21-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,1 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 72712-21:
(7*7)+(6*2)+(5*7)+(4*1)+(3*2)+(2*2)+(1*1)=111
111 % 10 = 1
So 72712-21-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O5/c1-7(13)10-4-5-11(16-8(2)14)12(6-10)17-9(3)15/h4-6H,1-3H3
72712-21-1Relevant articles and documents
Synthesis of catechols from phenols via Pd-catalyzed silanol-directed C-H oxygenation
Huang, Chunhui,Ghavtadze, Nugzar,Chattopadhyay, Buddhadeb,Gevorgyan, Vladimir
, p. 17630 - 17633 (2011/12/16)
A silanol-directed, Pd-catalyzed C-H oxygenation of phenols into catechols is presented. This method is highly site selective and general, as it allows for oxygenation of not only electron-neutral but also electron-poor phenols. This method operates via a silanol-directed acetoxylation, followed by a subsequent acid-catalyzed cyclization reaction into a cyclic silicon-protected catechol. A routine desilylation of the silacyle with TBAF uncovers the catechol product.
Studies on the Synthesis of Heterocyclic Compounds. XVI. Cleavage of 1,3-Benzodioxoles and -Benzoxathioles by Sodium Iodide-Acyl Chloride
Corda, Luciana,Fadda, Anna Maria,Maccioni, Antonio,Maccioni, Anna Maria,Podda, Gianni
, p. 311 - 314 (2007/10/02)
The cleavage reaction of ethereal and thioethereal bonds with sodium iodide and acyl chloride has been studied.In all the 1,3-benzodioxoles and -benzoxathioles studied, the opening of the heterocyclic ring with formation of 1,2-diacetoxybenzene or 2-hydroxythiophenol diacetic acid ester and gem-diiodoalkanes and iodoalkenes has been observed.The structure of newly prepared compounds has been determined by analytical and spectroscopic data or comparison with authentic samples.
