40073-83-4 Usage
Uses
Used in Food Industry:
2-FUROIC-D3 ACID is used as a preservative and flavoring agent for its ability to enhance the taste and extend the shelf life of food products. Its chemical properties allow it to maintain the freshness and quality of the products, making it a valuable addition to the food industry.
Used in Pharmaceutical Industry:
2-FUROIC-D3 ACID is used as a research compound for its potential applications in drug development and synthesis. Its unique chemical properties make it a valuable tool for studying various biological processes and developing new therapeutic agents.
Used in Chemical Research:
2-FUROIC-D3 ACID is used as a labeled compound in chemical research, allowing scientists to track and study the behavior of molecules in various chemical reactions and processes. Its stable isotopic labeling makes it an ideal candidate for such applications.
Used in Analytical Chemistry:
2-FUROIC-D3 ACID is used as a reference material in analytical chemistry for the calibration and validation of analytical instruments and methods. Its well-defined chemical properties make it a reliable standard for ensuring the accuracy and precision of measurements in various chemical analyses.
Check Digit Verification of cas no
The CAS Registry Mumber 40073-83-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,0,7 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 40073-83:
(7*4)+(6*0)+(5*0)+(4*7)+(3*3)+(2*8)+(1*3)=84
84 % 10 = 4
So 40073-83-4 is a valid CAS Registry Number.
40073-83-4Relevant academic research and scientific papers
σ-Bond initiated generation of aryl radicals from aryl diazonium salts
Chan, Bun,McErlean, Christopher S. P.,Nashar, Philippe E.,Tatunashvili, Elene
supporting information, p. 1812 - 1819 (2020/03/17)
σ-Bond nucleophiles and molecular oxygen transform aryl diazonium salts into aryl radicals. Experimental and computational studies show that Hantzsch esters transfer hydride to aryl diazonium species, and that oxygen initiates radical fragmentation of the diazene intermediate to produce aryl radicals. The operational simplicity of this addition-fragmentation process for the generation of aryl radicals, by a polar-radical crossover mechanism, has been illustrated in a variety of bond-forming reactions.
