CAS 41125-77-3
:5-(4-Nitrophenyl)-1,3,4-oxadiazol-2-ol
Description:
5-(4-Nitrophenyl)-1,3,4-oxadiazol-2-ol is a chemical compound characterized by its oxadiazole ring, which is a five-membered heterocyclic structure containing two nitrogen atoms and three carbon atoms. The presence of a nitrophenyl group at the 5-position contributes to its potential as a chromophore, influencing its electronic properties and reactivity. This compound typically exhibits a range of biological activities, making it of interest in medicinal chemistry and material science. Its hydroxyl group at the 2-position can participate in hydrogen bonding, enhancing its solubility and reactivity in various solvents. The nitro group is known for its electron-withdrawing properties, which can affect the compound's overall stability and reactivity. Additionally, 5-(4-Nitrophenyl)-1,3,4-oxadiazol-2-ol may exhibit fluorescence, making it useful in applications such as dye synthesis and as a probe in biological systems. As with many organic compounds, safety precautions should be taken when handling this substance due to potential toxicity associated with nitro-containing compounds.
Formula:C8H5N3O4
InChI:InChI=1S/C8H5N3O4/c12-8-10-9-7(15-8)5-1-3-6(4-2-5)11(13)14/h1-4H,(H,10,12)
InChI key:InChIKey=ADUFTMJBLYUADS-UHFFFAOYSA-N
SMILES:O=C1OC(C2=CC=C(N(=O)=O)C=C2)=NN1
Synonyms:- 5-(4-Nitrophenyl)-1,3,4-oxadiazol-2(3H)-one
- 5-(4-Nitrophenyl)-1,3,4-oxadiazol-2-ol
- D2-1,3,4-Oxadiazolin-5-one,2-(p-nitrophenyl)- (6CI)
- Δ<sup>2</sup>-1,3,4-Oxadiazolin-5-one, 2-(p-nitrophenyl)-
- Δ2-1,3,4-Oxadiazolin-5-one, 2-(p-nitrophenyl)-
- 1,3,4-Oxadiazol-2(3H)-one, 5-(4-nitrophenyl)-
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Found 2 products.
5-(4-Nitrophenyl)-1,3,4-oxadiazol-2-ol
CAS:Nitrophenols, such as 5-(4-nitrophenyl)-1,3,4-oxadiazol-2-ol (NPO), are a class of drugs that bind to the c1-6 alkyl receptor. This binding causes receptor desensitization and leads to the inhibition of the release of neurotransmitters such as acetylcholine, histamine, and serotonin. NPO is an excipient in some pharmaceuticals and may also be used for treatment of high blood pressure or damaged heart tissue. The carboxylic acid group on NPO can react with sodium ions to form a salt called sodium nitrophenolate. The residue from this reaction can be removed by adding a cationic polymer before use.
Formula:C8H5N3O4Purity:Min. 95%Molecular weight:207.14 g/mol
