CAS 108749-08-2

1,2,3,4-TETRAHYDRO-[2,7]NAPHTHYRIDINE

Description:

1,2,3,4-Tetrahydro-[2,7]naphthyridine is a bicyclic organic compound characterized by its fused ring structure, which includes a nitrogen atom in the heterocyclic framework. This compound belongs to the class of naphthyridines, which are derivatives of naphthalene with nitrogen atoms incorporated into the ring system. The presence of the tetrahydro group indicates that the compound is fully saturated, meaning it contains no double bonds within the ring structure. This saturation contributes to its stability and influences its reactivity. The compound is typically colorless to pale yellow and may exhibit a distinct odor. It is soluble in organic solvents, which is common for many nitrogen-containing heterocycles. 1,2,3,4-Tetrahydro-[2,7]naphthyridine has potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural similarity to biologically active compounds. Its properties, such as melting point, boiling point, and specific reactivity, can vary based on the presence of substituents and the conditions under which it is synthesized or utilized.

Formula: C₈H₁₀N₂

InChI: InChI=1/C8H10N2/c1-3-9-5-8-6-10-4-2-7(1)8/h1,3,5,10H,2,4,6H2

SMILES: c1cncc2CNCCc12

Synonyms:

• 2,7-Naphthyridine,1,2,3,4-tetrahydro-(9CI)
• 2,7-Naphthyridine, 1,2,3,4-tetrahydro
• 1,2,3,4-tetrahydro-2,7-Naphthyridine
• 1,2,3,4-Tetrahydro-2,7phthyridine
• 1,2,3,4-Tetrahydro-2,7-naphthyridine ,95%

1,2,3,4-Tetrahydro-2,7-naphthyridine

CAS: 108749-08-2

Formula: C₈H₁₀N₂

Color and Shape: Liquid

Molecular weight: 134.1784

Ref: IN-DA008XA8

1,2,3,4-Tetrahydro-2,7-naphthyridine

CAS: 108749-08-2

1,2,3,4-Tetrahydro-2,7-naphthyridine (1,2,3,4-THN) is a synthetic compound that can be made by the cross-coupling of an aryl halide with an organometallic reagent. It is used in the synthesis of polymers and as a precursor for pharmaceuticals. The reaction proceeds in two steps; first, deprotonation of the imine to form an enamine intermediate followed by intramolecular cyclization to produce 1,2,3,4-THN. This compound is hydrolyzed under acidic conditions to release methyl iodide and ammonia.

Formula: C₈H₁₀N₂

Purity: Min. 95.0 Area-%

Color and Shape: Clear Liquid

Molecular weight: 134.18 g/mol

Ref: 3D-FT141004