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59565-51-4

5-(2-Fluoro-phenyl)-[1,3,4]thiadiazol-2-ylamine

Catalog#: AR00EB6S  |   CAS#: 59565-51-4  |   MDL#: MFCD00981035  |   MF: C8H6FN3S  |   MW: 195.2167

Packsize Purity Price Availability Quantity
100mg 97% $7.00 Global Stock Buy Now Add To Cart
250mg 97% $14.00 Global Stock Buy Now Add To Cart
1g 97% $52.00 Global Stock Buy Now Add To Cart
5g 97% $259.00 Global Stock Buy Now Add To Cart
10g 97% $435.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00EB6S
Chemical Name 5-(2-Fluoro-phenyl)-[1,3,4]thiadiazol-2-ylamine
CAS Number 59565-51-4
Molecular Formula C8H6FN3S
Molecular Weight 195.2167
MDL Number MFCD00981035
SMILES Fc1ccccc1c1n[nH]c(=N)s1

5-(2-Fluorophenyl)-1,3,4-thiadiazol-2-amine, also known as $name$, serves as a valuable building block in chemical synthesis due to its versatile reactivity and unique structural features. This compound is widely utilized in organic chemistry for the development of new pharmaceuticals, agrochemicals, and materials.One key application of 5-(2-Fluorophenyl)-1,3,4-thiadiazol-2-amine in chemical synthesis is its use as a precursor for designing bioactive compounds. By incorporating this moiety into molecular structures, researchers can explore its potential as a pharmacophore, targeting specific biological pathways or receptors. Additionally, the presence of the fluorine atom in the phenyl ring confers enhanced lipophilicity and potentially improved pharmacokinetic properties to the resulting compounds.Furthermore, the thiodiazole core of 5-(2-Fluorophenyl)-1,3,4-thiadiazol-2-amine offers opportunities for diverse functionalization and derivatization. Chemists can introduce various substituents or modify the scaffold to fine-tune the physicochemical properties and biological activities of the synthesized molecules. This flexibility makes it a valuable tool for medicinal chemists and drug discovery programs aiming to develop novel therapeutics with improved efficacy and safety profiles.Overall, the strategic incorporation of 5-(2-Fluorophenyl)-1,3,4-thiadiazol-2-amine in chemical synthesis enables the construction of diverse molecular architectures with potential applications in drug development, agrochemical research, and material science. Its role as a key intermediate highlights its significance in advancing the field of organic chemistry and broadening the scope of scientific innovation.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class N/A
Packing Group N/A

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