4-chloroisoquinolin-7-amine

4-chloroisoquinolin-7-amine

1-chloro-4-fluoroisoquinoline

1-chloro-4-fluoroisoquinoline

7-nitroisoquinolin-4-amine

$300.00
CAS No.: 1936476-62-8
Catalog No.: 191967
Purity: 95%
MF: C9H7N3O2
MW: 189.174
Storage: 2-8 degree Celsius
SMILES: [N+](=O)([O-])C1=CC=C2C(=CN=CC2=C1)N
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191967
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7-nitroisoquinolin-4-amine; CAS No.: 1936476-62-8;7-nitroisoquinolin-4-amine. PROPERTIES: 7-nitroisoquinolin-4-amine is a heterocyclic aromatic compound with molecular formula C9H6N2O2. This crystalline solid exhibits typical properties of aromatic amines with a nitro group substituent. The 7-nitroisoquinolin-4-amine compound has a melting point ranging between 185-190 C and is moderately soluble in common polar solvents like dimethyl sulfoxide and dimethylformamide while showing limited solubility in water. The nitro group imparts strong electron-withdrawing characteristics, influencing the compound's reactivity and stability. Proper storage requires a tightly sealed container in a cool, dark environment below 20 C to prevent degradation. Safety precautions include using N-95 respiratory protection during handling, as the compound may pose inhalation hazards. Skin and eye contact should be avoided due to potential irritation. According to GHS standards, the compound carries H302+H312+H332 hazard statements for harmful effects via various exposure routes. APPLICATIONS: The 7-nitroisoquinolin-4-amine structure serves as a key intermediate in pharmaceutical synthesis pathways. In medicinal chemistry, it acts as a building block for developing isoquinoline-based alkaloid mimetics, as reported in heterocyclic chemistry journals. The compound's nitro group can be reduced to an amine functionality, enabling diverse synthetic transformations. Additionally, 7-nitroisoquinolin-4-amine derivatives have been investigated for their biological activities, particularly in antimicrobial and anticancer screening assays documented in medicinal research publications. The isoquinoline scaffold forms the basis for several FDA-approved medications, highlighting its importance in drug discovery pipelines according to pharmaceutical industry reports.

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