64822-00-0

Usage

Uses

Used in Pharmaceutical Industry:
1-(5-ANILINO-1,2,4-THIADIAZOL-3-YL)ACETONE is used as an intermediate in the synthesis of various drugs and pharmaceuticals for its ability to contribute to the development of medications with potent therapeutic effects.
Used in Cancer Treatment:
In the field of oncology, 1-(5-ANILINO-1,2,4-THIADIAZOL-3-YL)ACETONE is utilized as an anti-cancer agent, targeting a range of malignancies due to its inherent biological activities that can inhibit tumor growth and progression.
Used in Inflammation and Infection Management:
1-(5-ANILINO-1,2,4-THIADIAZOL-3-YL)ACETONE is employed as an anti-inflammatory and anti-bacterial agent, making it a potential candidate for the development of treatments aimed at reducing inflammation and combating bacterial infections.
Used in Dye and Pigment Production:
This chemical compound is also used as a key component in the development of dyes, pigments, and other organic compounds, highlighting its versatility in various industrial applications.
Used in Material Science and Chemical Research:
1-(5-ANILINO-1,2,4-THIADIAZOL-3-YL)ACETONE has been studied for its potential applications in material science and chemical research, where it may contribute to the advancement of novel materials and chemical processes.

Upstream product

• 1072-67-9 5-methylisoxazol-3-ylamine 
• 103-71-9 phenyl isocyanate 
• 321309-33-5 5-methylisoxazolyl-3-isothiocyanate 
• 62-53-3 aniline 
• 103-72-0 phenyl isothiocyanate 
• 64821-97-2 1-(5-methylisoxazol-3-yl)-3-phenylthiourea 

Downstream Products

• 1245618-40-9 1-[(5-phenylamino)-1,2,4-thiadiazol-3-yl]propan-2-ol 
• 667428-74-2 [3-(1'-phenylethylaminopropenyl)-1,2,4-thiadiazol-5-yl]phenylamine 
• 1415982-92-1 [3-(1'-phenylethylaminopropyl)-1,2,4-thiadiazol-5-yl]phenylamine 

Relevant academic research and scientific papers

1-(5-(R-Amino)-1,2,4-thiadiazol-3-yl)propan-2-ones: Convenient ketomethylenic reagents for the gewald and dimroth reactions

1-(5-(R-Amino)-1,2,4-thiadiazol-3-yl)propan-2-ones were used as activated ketomethylenic compounds for the Gewald and Dimroth reactions. It was found out that they exhibited high reactivity in such anion reactions for the construction of the 1,2,3-triazol

Novel 1,2,4-thiadiazole derivatives as potent neuroprotectors: Approach to creation of bioavailable drugs

Novel 1,2,4-thiadiazole derivatives as potent neuroprotectors were synthesized and identified. Their ability to inhibit the glutamate stimulated Ca uptake was measured. Permeation experiments on the phospholipid membranes were conducted, and the apparent

Mononuclear heterocyclic rearrangements. Part 11. Rearrangements of 1,2,4-oxadiazoles, isoxazoles, and 1,2,5-oxadiazoles involving a sulphur atom

The reactions of 3-amino-5-methyl- and 3-amino-5-phenyl-1,2,4-oxadiazoles, 3-amino-5-methylisoxazole, and 3-amino-4-methyl- and 3-amino-4-phenyl-1,2,5- oxadiazoles with phenyl isothiocyanate have been investigated, and the reactivity of phenylthioureido-derivatives (3) of these ring systems towards rearrangement have been studied. The presence of a sulphur atom in the side-chain sequence (1; XYZ = NCS) greatly enhances the reactivity of the systems under consideration towards rearrangement. The tendency of the three heterocycles to rearrange decreases in the order 1,2,4-oxadiazole > isoxazole > 1,2,5-oxadiazole.