5202-32-4 Usage
Uses
Used in Food and Beverage Industry:
2,3,4-Furantricarboxylic acid, 5-methoxy-, trimethyl ester is used as a flavoring agent and preservative in the food and beverage industry. Its unique properties help enhance the taste and extend the shelf life of various products.
Used in Pharmaceutical Production:
2,3,4-Furantricarboxylic acid, 5-methoxy-, trimethyl ester is utilized in the production of pharmaceuticals, where it serves as a key ingredient in the development of drugs with potential health benefits.
Used as a Chemical Intermediate in Organic Synthesis:
2,3,4-Furantricarboxylic acid, 5-methoxy-, trimethyl ester is employed as a chemical intermediate in organic synthesis, playing a crucial role in the synthesis of various organic compounds.
While the provided materials do not explicitly mention specific applications in different industries beyond the general uses listed, the compound's versatility in the food and beverage industry, pharmaceutical production, and organic synthesis highlights its potential for diverse applications. Further research and development may reveal additional uses and benefits of 2,3,4-Furantricarboxylic acid, 5-methoxy-, trimethyl ester in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5202-32-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,0 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5202-32:
(6*5)+(5*2)+(4*0)+(3*2)+(2*3)+(1*2)=54
54 % 10 = 4
So 5202-32-4 is a valid CAS Registry Number.
5202-32-4Relevant academic research and scientific papers
Synthesis and reactivity of a novel group of hydroxylamine-containing 2π- and 4π-components
Pearce, Alan J.,Walter, Daryl S.,Frampton, Christopher S.,Gallagher, Timothy
, p. 847 - 852 (2007/10/03)
The synthesis of hydroxylamine-based reagents, alkene 2, alkyne 3 and a butadienyl variant pyrone 4 are described. While the relative instability of alkyne 3 has limited further evaluation, alkene 2 and pyrone 4 successfully participate in 1,3-dipolar and Diels-Alder cycloaddition reactions respectively. Reaction of 4 with DMAD gives O-arylated hydroxylamine 13, the structure of which is confirmed by crystallographic analysis.
