42528-99-4 Usage
Description
4-(2-acetoxyacetyl)phenyl acetate is an organic compound that serves as a versatile reagent in the synthesis of various glycol metabolites. It is characterized by its acetoxyacetyl and phenyl acetate functional groups, which contribute to its reactivity and utility in chemical reactions.
Uses
Used in Chemical Synthesis:
4-(2-acetoxyacetyl)phenyl acetate is used as a general reagent for the synthesis of glycol metabolites. Its unique structure allows it to participate in a range of chemical reactions, facilitating the production of various glycol-based compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-(2-acetoxyacetyl)phenyl acetate is used as a key intermediate in the synthesis of drugs targeting glycolysis pathways. Its ability to form glycol metabolites makes it a valuable component in the development of therapeutic agents for conditions related to glycolytic dysregulation.
Used in Research and Development:
4-(2-acetoxyacetyl)phenyl acetate is also utilized in research and development settings, where it aids in the study of glycolysis and the development of novel compounds with potential applications in medicine and biotechnology. Its role in the synthesis of glycol metabolites makes it an essential tool for scientists working on related projects.
Check Digit Verification of cas no
The CAS Registry Mumber 42528-99-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,5,2 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 42528-99:
(7*4)+(6*2)+(5*5)+(4*2)+(3*8)+(2*9)+(1*9)=124
124 % 10 = 4
So 42528-99-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H12O5/c1-8(13)16-7-12(15)10-3-5-11(6-4-10)17-9(2)14/h3-6H,7H2,1-2H3
42528-99-4Relevant articles and documents
Carboxylic acid derivative compound and its preparation method and application
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Paragraph 0089; 0090, (2017/01/31)
The invention provides a carboxylic acid derivative compound. The compound as shown in the formula (I) or the pharmaceutically acceptable salt thereof provided by the invention not only can reduce the level of triglyceride in high fat model animal blood, but also has the good function of reducing cholesterol and low-density lipoprotein and the effects of promoting biliation, reducing content of cholesterol in bile and increasing the content of bile acid, and also has the effect of preventing and treating gallstone when being applied to a golden gopher gallstone model. The particular importance is that the compound or the pharmaceutically acceptable salt thereof provided by the invention is low in toxicity.
Synthesis of [4-14C]-pelargonidin chloride and [4- 14C]-delphinidin chloride
Kraus, Michael,Biskup, Ellen,Richling, Elke,Schreier, Peter
, p. 1151 - 1162 (2007/10/03)
The synthesis of [4-14C]-pelargonidin chloride and [4- 14C]-delphinidin chloride via [formyl-14C]-2-(benzoyloxy)- 4,6-dihydroxybenzaldehyde, ω,4-diacetoxyacetophenone and ω,3,4,5-tetraacetoxyacetophenone is described. The first step comprised labelling of the carbonyl group of 2-(benzoyloxy)-4,6-dihydroxybenzaldehyde, verifying that the coupling with ω,4-diacetoxyacetophenone or ω,3,4,5-tetraacetoxyacetophenone under hydrogen chloride atmosphere resulted in the formation of [4-14C] labelled anthocyanidins. Copyright
