79694-16-9 Usage
Uses
Used in Scientific Research:
4-Propoxylmandelic acid is used as a research compound for conducting various types of experiments in the fields of biology and pharmaceuticals. It aids in the investigation of different biological processes and the development of new pharmaceutical agents.
Used in Laboratory Settings:
4-Propoxylmandelic acid is used as a laboratory reagent for facilitating the execution of scientific studies. Its synthetic nature allows researchers to control the experimental conditions and better understand the outcomes of their research.
Used in Pharmaceutical Studies:
4-Propoxylmandelic acid is used as a potential drug candidate in pharmaceutical research. It may contribute to the discovery of new therapeutic agents or the enhancement of existing ones, although further investigation is required to determine its efficacy and safety.
Used in Biological Studies:
4-Propoxylmandelic acid is used as a biological probe in studies aimed at understanding complex biological systems. It can help researchers identify and characterize the mechanisms underlying certain biological phenomena.
Check Digit Verification of cas no
The CAS Registry Mumber 79694-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,9 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 79694-16:
(7*7)+(6*9)+(5*6)+(4*9)+(3*4)+(2*1)+(1*6)=189
189 % 10 = 9
So 79694-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H14O4/c1-2-7-15-9-5-3-8(4-6-9)10(12)11(13)14/h3-6,10,12H,2,7H2,1H3,(H,13,14)
79694-16-9Relevant academic research and scientific papers
Kinetic resolution of mandelate esters via stereoselective acylation catalyzed by lipase PS-30
Chen, Peiran,Yang, Wenhong
supporting information, p. 2290 - 2294 (2014/04/17)
By using lipase PS-30 as catalyst, the kinetic resolution of a series of racemic mandelate esters has been achieved via stereoselective acylation. The value of kinetic enantiomeric ratio (E) reached up to 197.5. Substituent effect is briefly discussed.
ALPHA-HYDROXY-BENZENEACETIC ACID DERIVATIVES, AND COMPOUNDS HAVING TWO 5-MEMBERED LACTONE RINGS FUSED TO CENTRAL CYCLOHEXA-1,4-DIENE NUCLEUS BASED UPON THE SAME, AND USES OF THE COMPOUNDS
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Page/Page column 34, (2008/06/13)
The present invention provides a-hydroxy benzeneacetic acid derivatives of the formula as defined in the specification which is a precursor indispensable for synthesis of compounds having two 5-membered lactone rings fused to central cyclohexa-1,4-dien
