CAS 931-07-7
:4-Nitroisothiazole
Description:
4-Nitroisothiazole is a heterocyclic organic compound characterized by a five-membered ring containing both sulfur and nitrogen atoms, specifically featuring a nitro group (-NO2) at the 4-position of the isothiazole ring. This compound typically appears as a yellow to orange crystalline solid and is known for its aromatic properties, which contribute to its stability and reactivity. It is soluble in organic solvents but has limited solubility in water. 4-Nitroisothiazole is utilized in various applications, including as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes. Its chemical structure allows for potential electrophilic substitution reactions, making it a valuable building block in organic synthesis. Additionally, the presence of the nitro group can impart unique electronic properties, influencing the compound's reactivity and interactions with other chemical species. Safety precautions should be observed when handling this compound, as nitro-containing compounds can be hazardous and may pose environmental risks.
Formula:C3H2N2O2S
InChI:InChI=1S/C3H2N2O2S/c6-5(7)3-1-4-8-2-3/h1-2H
InChI key:InChIKey=FNXPAYVHLSTHQY-UHFFFAOYSA-N
SMILES:N(=O)(=O)C=1C=NSC1
Synonyms:- 4-Nitroisothiazole
- Isothiazole, 4-nitro-
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Found 4 products.
4-Nitroisothiazole
CAS:<p>4-Nitroisothiazole is a nitro derivative of isothiazole that has been shown to have inhibitory effects on bacterial growth. It has been shown to be active against the gram-positive bacterium, Staphylococcus aureus, and the gram-negative bacterium Escherichia coli. 4-Nitroisothiazole inhibits the growth of bacteria by binding to the cytoplasmic membrane, leading to an increase in the redox potential and preventing electron transport. 4-Nitroisothiazole also inhibits cellular respiration and protein synthesis, which leads to cell death.</p>Formula:C3H2N2O2SPurity:Min. 95%Molecular weight:130.13 g/mol
