19054-27-4 Usage
Uses
Used in Pharmaceutical Industry:
2-Acetyl-3,5-dihydroxyphenylacetic acid ethyl ester is used as an intermediate compound for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Chemical Research:
In the field of chemical research, 2-Acetyl-3,5-dihydroxyphenylacetic acid ethyl ester serves as a valuable compound for studying the properties and reactivity of phenolic esters. It can be used to explore new reaction mechanisms, develop novel synthetic methods, and investigate the effects of structural modifications on the compound's properties.
Used in Antimicrobial Applications:
Curvulin, a compound isolated from the extract of the plant-associated fungus Chaetosphaeronema achilleae, is an antimicrobial agent. 2-Acetyl-3,5-dihydroxyphenylacetic acid ethyl ester may be used as a structural analog or precursor in the development of new antimicrobial agents, potentially enhancing their efficacy against various pathogens.
Used in Drug Delivery Systems:
Similar to gallotannin, 2-Acetyl-3,5-dihydroxyphenylacetic acid ethyl ester could be employed in the development of novel drug delivery systems. Its unique chemical structure may allow for the design of targeted drug carriers, improving the bioavailability and therapeutic outcomes of associated pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 19054-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,5 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19054-27:
(7*1)+(6*9)+(5*0)+(4*5)+(3*4)+(2*2)+(1*7)=104
104 % 10 = 4
So 19054-27-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O5/c1-3-17-11(16)5-8-4-9(14)6-10(15)12(8)7(2)13/h4,6,14-15H,3,5H2,1-2H3
19054-27-4Relevant academic research and scientific papers
Aryne acyl-alkylation in the general and convergent synthesis of benzannulated macrolactone natural products: An enantioselective synthesis of (-)-curvularin
Tadross, Pamela M.,Virgil, Scott C.,Stoltz, Brian M.
supporting information; experimental part, p. 1612 - 1614 (2010/06/17)
(Figure Presented) A general approach for the synthesis of benzannulated macrolactone natural products utilizing an ary ne acyl-alkylation reaction is described. Toward this end, the total syntheses of the natural products (-)-curvularin, curvulin, and (-
