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Home  > 5-(4-Fluorophenyl)-1,2,4-thiadiazol-3-amine

AE20060

1086385-83-2 | 5-(4-Fluorophenyl)-1,2,4-thiadiazol-3-amine

Packsize Purity Availability Price Discounted Price    Quantity
1mg 95% 3 weeks $747.00 $523.00 -   +
5mg 95% 3 weeks $843.00 $590.00 -   +
10mg 95% 3 weeks $912.00 $639.00 -   +
25mg 95% 3 weeks $1,160.00 $812.00 -   +
50mg 95% 3 weeks $1,677.00 $1,174.00 -   +
1g 95% 3 weeks $2,324.00 $1,627.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE20060
Chemical Name: 5-(4-Fluorophenyl)-1,2,4-thiadiazol-3-amine
CAS Number: 1086385-83-2
Molecular Formula: C8H6FN3S
Molecular Weight: 195.2167
MDL Number: MFCD11655561
SMILES: Fc1ccc(cc1)c1snc(n1)N

 

Upstream Synthesis Route
  • 5-(4-Fluorophenyl)-1,2,4-thiadiazol-3-amine is a valuable compound used in chemical synthesis due to its versatile reactivity and unique structural features. It serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and materials.One of the primary applications of 5-(4-Fluorophenyl)-1,2,4-thiadiazol-3-amine in chemical synthesis is as a precursor for the preparation of novel heterocyclic compounds. By undergoing various reactions such as substitution, oxidation, and coupling, this compound can be transformed into a wide range of functionalized molecules with diverse properties and applications.Additionally, 5-(4-Fluorophenyl)-1,2,4-thiadiazol-3-amine can be utilized in the construction of molecular scaffolds for drug discovery and development. Its unique heterocyclic structure offers opportunities for the design of potential pharmaceutical agents targeting specific biological pathways or disease mechanisms.Furthermore, this compound can be employed in the synthesis of advanced materials with tailor-made properties, such as conductive polymers, luminescent compounds, or molecular sensors. Its presence in the molecular structure imparts desirable characteristics to the final material, enabling applications in electronics, optics, and sensing technologies.Overall, the versatile reactivity and synthetic utility of 5-(4-Fluorophenyl)-1,2,4-thiadiazol-3-amine make it a valuable tool for chemists and researchers seeking to access diverse chemical space and develop innovative compounds for various industrial and scientific applications.
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