CAS 80957-68-2

5,6,7,8-Tetrahydro-1,6-naphthyridine

Description:

5,6,7,8-Tetrahydro-1,6-naphthyridine is a bicyclic organic compound characterized by its fused ring structure, which includes a nitrogen atom in the naphthyridine framework. This compound features a saturated tetrahydro configuration, indicating the presence of four hydrogen atoms that contribute to its stability and reactivity. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of the nitrogen atom in the ring system imparts basic properties, allowing it to participate in various chemical reactions, including nucleophilic substitutions and coordination with metal ions. This compound is of interest in medicinal chemistry due to its potential biological activities, including antimicrobial and anti-inflammatory properties. Its derivatives may also exhibit pharmacological effects, making it a subject of research in drug development. As with many nitrogen-containing heterocycles, it may also serve as a building block for synthesizing more complex molecules in organic synthesis. Safety data should be consulted for handling and storage, as with all chemical substances.

Formula: C₈H₁₀N₂

Synonyms:

• 1,6-Naphthyridine,5,6,7,8-tetrahydro-
• 5,6,7,8-tetrahydro-1,6-naphthyridine HCl Salt
• 5,6,7,8-TETRAHYDRO-[1,6]NAPHTHYRIDINE
• 5,6,7,8-Tetrahydro-1,6phthyridine
• 5,6,7,8-tetrahydro-1,6-naphthyridine(SALTDATA: 2HCl 0.5H2O)

1,6-Naphthyridine, 5,6,7,8-tetrahydro-

CAS: 80957-68-2

Formula: C₈H₁₀N₂

Purity: 96%

Color and Shape: Solid

Molecular weight: 134.1784

Ref: IN-DA00ID5E

5,6,7,8-Tetrahydro-1,6-naphthyridine

CAS: 80957-68-2

5,6,7,8-Tetrahydro-1,6-naphthyridine

Purity: 97%

Molecular weight: 134.18g/mol

Ref: 54-OR77184

5,6,7,8-Tetrahydro-1,6-naphthyridine

CAS: 80957-68-2

Formula: C₈H₁₀N₂

Purity: 95%

Color and Shape: Powder

Molecular weight: 134.182

Ref: 10-F076900

5,6,7,8-Tetrahydro-1,6-naphthyridine

CAS: 80957-68-2

The compound 5,6,7,8-tetrahydro-1,6-naphthyridine is a potent inhibitor of the integrase enzyme. This compound has been shown to have a cytotoxic effect on cells in culture and has been found to inhibit replication of HIV and herpes simplex virus type 1. The cytotoxic effect of this compound may be due to its ability to inhibit the growth factor receptor. The benzimidazole derivative has a boronic acid group that can form a covalent bond with an amide group on the protein receptor. This bond inhibits the binding of the ligand to the protein receptor and prevents cell proliferation.

Formula: C₈H₁₀N₂

Purity: Min. 95%

Molecular weight: 134.18 g/mol

Ref: 3D-FT143759