68029-49-2 Usage
Uses
Used in Organic Synthesis:
(E)-3-(2-furyl)-2-cyanoprop-2-enethioamide is utilized as a key intermediate in organic synthesis, playing a crucial role in the creation of various complex organic molecules. Its unique structure allows for multiple reaction pathways, making it a valuable component in the synthesis of a wide array of compounds.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, (E)-3-(2-furyl)-2-cyanoprop-2-enethioamide serves as an intermediate for the production of different medicinal compounds. Its structural features facilitate the development of new drugs with potential therapeutic applications.
Used in Antimicrobial Applications:
(E)-3-(2-furyl)-2-cyanoprop-2-enethioamide is used as an antimicrobial agent due to its ability to inhibit the growth of certain microorganisms. This property makes it a candidate for further research and development in the fight against bacterial and fungal infections.
Used in Anti-Fungal Applications:
Similarly, its antifungal properties position (E)-3-(2-furyl)-2-cyanoprop-2-enethioamide as a potential agent in the treatment and prevention of fungal infections, offering a new avenue for pharmaceutical research.
Used in Pesticide and Insecticide Development:
(E)-3-(2-furyl)-2-cyanoprop-2-enethioamide has also been studied for its potential as a pesticide and insecticide. Its ability to deter or kill pests could make it a valuable tool in agriculture for protecting crops and increasing yield.
Check Digit Verification of cas no
The CAS Registry Mumber 68029-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,2 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68029-49:
(7*6)+(6*8)+(5*0)+(4*2)+(3*9)+(2*4)+(1*9)=142
142 % 10 = 2
So 68029-49-2 is a valid CAS Registry Number.
68029-49-2Relevant academic research and scientific papers
N-Hydroxymethylation of 3-Aryl-2-cyanoprop-2-enethioamides
Chigorina, E. A.,Dotsenko, V. V.,Krivokolysko, S. G.
, p. 1411 - 1417 (2020/09/21)
Abstract: Hydroxymethylation of (E)-3-aryl-2-cyanoprop-2-enethioamides with an aqueous alcoholic solution of formaldehyde has afforded (E)-3-aryl-N-(hydroxymethyl)-2-cyanoprop-2-enethioamides. The predictive analysis of the biological activity of the obtained compounds in silico has been carried out.
