CAS 17647-71-1
:1-(4-Amino-1,2,5-oxadiazol-3-yl)ethanone
Description:
1-(4-Amino-1,2,5-oxadiazol-3-yl)ethanone, with CAS number 17647-71-1, is a chemical compound characterized by its oxadiazole ring structure, which contributes to its unique properties. This compound features an amino group and an ethanone moiety, making it a potential candidate for various applications in medicinal chemistry and material science. The presence of the oxadiazole ring imparts notable stability and may enhance its biological activity, particularly in the context of antimicrobial or antitumor properties. The compound is typically synthesized through specific organic reactions that involve the introduction of the amino group and the carbonyl functionality. Its solubility and reactivity can vary depending on the solvent and conditions used, which is important for its application in research and development. Additionally, the compound's structure allows for potential modifications that could lead to derivatives with enhanced efficacy or selectivity in biological systems. Overall, 1-(4-Amino-1,2,5-oxadiazol-3-yl)ethanone is of interest in various fields due to its distinctive chemical features.
Formula:C4H5N3O2
InChI:InChI=1S/C4H5N3O2/c1-2(8)3-4(5)7-9-6-3/h1H3,(H2,5,7)
InChI key:InChIKey=RFLWXQYQVUNPBF-UHFFFAOYSA-N
SMILES:C(C)(=O)C=1C(N)=NON1
Synonyms:- 1,2,5-Oxadiazole, ethanone deriv.
- 1-(4-Amino-1,2,5-Oxadiazol-3-Yl)Ethanone
- 1-(4-Amino-1,2,5-oxadiazol-3-yl)ethan-1-one
- Ethanone, 1-(4-amino-1,2,5-oxadiazol-3-yl)-
- Ketone, 4-amino-3-furazanyl methyl
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Found 1 products.
1-(4-Amino-1,2,5-oxadiazol-3-yl)ethan-1-one
CAS:<p>Versatile small molecule scaffold</p>Formula:C4H5N3O2Purity:Min. 95%Molecular weight:127.1 g/mol
