108474-23-3 Usage
Uses
Used in Pharmaceutical Industry:
2,6-dimethoxyphenyl benzoate is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs and enhance the properties of existing ones.
Used in Organic Synthesis:
2,6-dimethoxyphenyl benzoate is used as a reagent in organic synthesis for the preparation of esters and other organic compounds, facilitating the creation of a wide range of chemical products.
Used in Photoluminescent Materials:
2,6-dimethoxyphenyl benzoate is studied for its potential use in photoluminescent materials, indicating its possible application in the development of advanced optical and electronic devices.
Used in Anti-inflammatory Research:
2,6-dimethoxyphenyl benzoate is explored as a potential anti-inflammatory agent, suggesting its future use in the medical field for treating inflammation-related conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 108474-23-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,4,7 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 108474-23:
(8*1)+(7*0)+(6*8)+(5*4)+(4*7)+(3*4)+(2*2)+(1*3)=123
123 % 10 = 3
So 108474-23-3 is a valid CAS Registry Number.
108474-23-3Relevant academic research and scientific papers
Electrodimerization of N-Alkoxyamides for Zinc(II) Catalyzed Phenolic Ester Synthesis under Mild Reaction Conditions
Subramanian, Kripa,Yedage, Subhash L.,Bhanage, Bhalchandra M.
, p. 2511 - 2521 (2018/05/14)
An electrochemical On-Off method for phenolic ester synthesis from N-alkoxyamides has been reported. This one-pot protocol begins with rapid and selective electrodimerization of the amide using n-Bu4NI (TBAI) as an electrocatalyst. The reaction proceeds further in the absence of current via Zn catalyzed C?N bond activation of the amide dimer followed by its coupling with phenol to form the ester. The present methodology is ligand-free and takes place under mild reaction conditions. This transformation incorporates a wide variety of phenols and amide substrates leading to the formation of functionalized esters highlighting its versatility. (Figure presented.).
