CAS 42606-39-3

8-Nitro-5-quinolinamine

Description:

8-Nitro-5-quinolinamine is an organic compound characterized by its quinoline structure, which consists of a bicyclic aromatic system containing a nitrogen atom. The presence of a nitro group at the 8-position and an amino group at the 5-position contributes to its unique chemical properties. This compound typically exhibits a yellow to orange color and is soluble in organic solvents, while its solubility in water may vary. It is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its ability to interact with biological targets. The nitro group can participate in various chemical reactions, making it a versatile intermediate in organic synthesis. Additionally, the compound may exhibit biological activity, including antimicrobial or anticancer properties, although specific biological effects would depend on further research. Safety data should be consulted, as nitro compounds can be hazardous and may require appropriate handling and storage precautions.

Formula: C₉H₇N₃O₂

InChI: InChI=1S/C9H7N3O2/c10-7-3-4-8(12(13)14)9-6(7)2-1-5-11-9/h1-5H,10H2

InChI key: InChIKey=HUJXJGQTEDKYER-UHFFFAOYSA-N

SMILES: N(=O)(=O)C=1C2=C(C(N)=CC1)C=CC=N2

Synonyms:

• 5-Amino-8-nitroquinoline
• 5-Quinolinamine, 8-nitro-
• 8-Nitro-5-quinolinamine

8-Nitroquinolin-5-amine

CAS: 42606-39-3

8-Nitroquinolin-5-amine is a quinoline derivative that undergoes electrophilic substitution reactions with nucleophiles. This drug reacts with hydrogen chloride to give the corresponding 8-nitroquinolinium chloride. Reaction of this compound with imines gives the corresponding imine derivatives. Reaction of this compound with chlorides gives the corresponding 8-nitroquinolinium salts. The reactivity of this compound is similar to that of quinones, but it does not have a conjugated system and is not redox active.

Formula: C₉H₇N₃O₂

Purity: Min. 95%

Molecular weight: 189.17 g/mol

Ref: 3D-SBA60639