2826-31-5 Usage
Uses
Used in Analytical Chemistry:
(2-ethoxybenzylidene)propanedinitrile is used as a fluorescent detection reagent for the quantification of cyanide ions in aqueous solutions due to its high sensitivity and selectivity towards cyanide ions.
Used in Environmental Monitoring:
(2-ethoxybenzylidene)propanedinitrile is used as a tool for monitoring cyanide levels in the environment, helping to ensure safety and compliance with environmental regulations.
Used in Optical Sensors Development:
(2-ethoxybenzylidene)propanedinitrile is used in the development of optical sensors for cyanide detection, providing a potential advancement in sensor technology for environmental and industrial applications.
Used in Dye Production:
(2-ethoxybenzylidene)propanedinitrile is used as a chemical intermediate in the production of dyes, contributing to the color and properties of various dye products.
Used in Pharmaceutical Industry:
(2-ethoxybenzylidene)propanedinitrile is used in the production of pharmaceuticals, potentially playing a role in the development of new drugs and treatments.
Used in Organic Synthesis:
(2-ethoxybenzylidene)propanedinitrile is used as a reagent in organic synthesis, enabling the creation of a variety of organic compounds for research and commercial purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 2826-31-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,2 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2826-31:
(6*2)+(5*8)+(4*2)+(3*6)+(2*3)+(1*1)=85
85 % 10 = 5
So 2826-31-5 is a valid CAS Registry Number.
2826-31-5Relevant academic research and scientific papers
An efficient five-component synthesis of thioether containing dihydropyrano[2,3-c]pyrazoles: a green domino strategy
Ramesh, Vediyappan,Shanmugam, Sivakumar,Devi, Natarajan Savitha
, p. 9993 - 10001 (2016/12/07)
An efficient route for the synthesis of novel thioether containing dihydropyrano[2,3-c]pyrazoles has been accomplished via a solvent-free, catalyst-free, one-pot, five component domino strategy. This synthetic approach offers several advantages such as an easy work-up, no need for purification techniques and a short reaction time with good atom economy and high yields of the products (81-86%).
