
CAS 20141-83-7
:7-Nitroisoquinolin-1(2H)-one
Description:
7-Nitroisoquinolin-1(2H)-one is a heterocyclic organic compound characterized by its isoquinoline structure, which includes a nitrogen atom in the aromatic ring. This compound features a nitro group (-NO2) at the 7-position and a keto group (C=O) at the 1-position of the isoquinoline framework. It is typically a yellow to orange crystalline solid, exhibiting moderate solubility in organic solvents. The presence of the nitro group contributes to its potential reactivity and makes it a subject of interest in various chemical applications, including medicinal chemistry and material science. The compound may exhibit biological activity, making it relevant in pharmacological studies. Its molecular structure allows for various functionalization possibilities, which can lead to derivatives with enhanced properties. As with many nitro-containing compounds, it is important to handle 7-nitroisoquinolin-1(2H)-one with care due to potential toxicity and environmental considerations.
Formula:C9H6N2O3
Synonyms:- 7-nitro-2H-isoquinolin-1-one
- 7-Nitroisoquinolin-1(2H)
- 7-Nitroisoquinolin-1(2H)-one
- 7-Nitroisocarbostyril
- 1(2H)-Isoquinolinone, 7-nitro-
- 7-Nitroisoquinolin-1-ol
- 7-Nitro-1(2H)-isoquinolinone
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Found 4 products.
1(2H)-Isoquinolinone, 7-nitro-
CAS:Formula:C9H6N2O3Purity:95%Color and Shape:SolidMolecular weight:190.15557-Nitroisoquinolin-1(2H)-one
CAS:<p>7-Nitroisoquinolin-1(2H)-one</p>Purity:97%Molecular weight:190.16g/mol7-Nitroisoquinolin-1(2H)-one
CAS:Formula:C9H6N2O3Purity:96%Color and Shape:SolidMolecular weight:190.1587-Nitroisoquinolin-1(2H)-one
CAS:<p>7-Nitroisoquinolin-1(2H)-one is a chemical compound that can be obtained by reacting n-alkyl chloride with nitric acid. This reaction yields 7-nitroisoquinolin-1(2H)-one in a sequence of steps, which begins by the formation of nitrous acid and the nitration of an alcohol to form an alkyl nitrate. The next step involves the reaction of an alkyl nitrate with hydrochloric acid to form an alkyl chloride, followed by a second reaction with hydrochloric acid to form the final product.</p>Formula:C9H6N2O3Purity:Min. 95%Molecular weight:190.16 g/mol



