126335-03-3 Usage
Uses
Used in Pharmaceutical Development:
(2E)-3-[(4-amino-4H-1,2,4-triazol-3-yl)sulfanyl]-1-phenylprop-2-en-1-one is used as a key intermediate in the synthesis of pharmaceuticals for the treatment of various diseases and conditions. Its triazolylsulfanyl group is known to be effective in certain therapeutic applications, making (2E)-3-[(4-amino-4H-1,2,4-triazol-3-yl)sulfanyl]-1-phenylprop-2-en-1-one a valuable asset in medicinal chemistry.
Used in Agriculture:
In the agricultural industry, (2E)-3-[(4-amino-4H-1,2,4-triazol-3-yl)sulfanyl]-1-phenylprop-2-en-1-one may be utilized for the development of agrochemicals, such as pesticides or herbicides, due to its unique chemical structure and potential bioactivity.
Used in Materials Science:
(2E)-3-[(4-amino-4H-1,2,4-triazol-3-yl)sulfanyl]-1-phenylprop-2-en-1-one could also be employed in materials science for the creation of novel materials with specific properties, such as those with antimicrobial or other functional attributes, depending on further research into its characteristics and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 126335-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,3,3 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 126335-03:
(8*1)+(7*2)+(6*6)+(5*3)+(4*3)+(3*5)+(2*0)+(1*3)=103
103 % 10 = 3
So 126335-03-3 is a valid CAS Registry Number.
126335-03-3Relevant academic research and scientific papers
SYNTHESIS OF 1,2,4-TRIAZOLO-1,3,4-THIADIAZEPINES AND 4-AMINO-3-ACYLVINYLTHIO-1,2,4-TRIAZOLES BY REACTION O ACYLACETYLENES WITH 4-AMINO-3-MERCAPTO-1,2,4-TRIAZOLE
Glotova, T. E.,Nakhmanovich, A. S.,Romanenko, L. S.,Sigalov, M. V.
, p. 795 - 798 (2007/10/02)
1,2,4-Triazolo-1,3,4-thiadiazepines have been prepared by treating α-acetylenic ketones with 4-amino-3-mercapto-1,2,4-triazole in glacial acetic acid.Terminal acetylenic ketones react with the triazole to form 4-amino-3-acylvinylthio-1,2,4-triazoles.Heating the latter with hydrazine hydrate in alcohol yields substituted pyrazoles.
