CAS 487-10-5

1,2-Di-1-naphthalenyldiazene

Description:

1,2-Di-1-naphthalenyldiazene, with the CAS number 487-10-5, is an organic compound characterized by its structure, which features two naphthalene moieties connected by a diazene (-N=N-) linkage. This compound is typically a solid at room temperature and exhibits a deep color, often associated with its conjugated system, which can absorb light in the visible spectrum. The presence of the diazene group imparts unique chemical reactivity, particularly in terms of its ability to undergo azo coupling reactions, making it of interest in synthetic organic chemistry. Additionally, 1,2-Di-1-naphthalenyldiazene may exhibit interesting photophysical properties, such as fluorescence or phosphorescence, due to its extended π-conjugation. Its stability can be influenced by factors such as temperature and the presence of solvents, and it may be sensitive to light, leading to potential degradation. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if inhaled or ingested.

Formula: C₂₀H₁₄N₂

InChI: InChI=1/C20H14N2/c1-3-11-17-15(7-1)9-5-13-19(17)21-22-20-14-6-10-16-8-2-4-12-18(16)20/h1-14H/b22-21+

InChI key: InChIKey=ICIDZHMCYAIUIJ-UHFFFAOYSA-N

SMILES: N(=NC=1C2=C(C=CC1)C=CC=C2)C=3C4=C(C=CC3)C=CC=C4

Synonyms:

• (E)-dinaphthalen-1-yldiazene
• 1,1'-Azobisnaphthalene
• 1,1'-Azonaphthalene
• 1,2-Di-1-naphthalenyldiazene
• Brn 0959427
• Di-1-naphthyldiazene
• Diazene, 1,2-di-1-naphthalenyl-
• Diazene, di-1-naphthalenyl-
• Diazene, di-1-naphthalenyl- (9CI)
• Nsc 113051
• 2-16-00-00026 (Beilstein Handbook Reference)
• Azonaphthalene
• 1,2-Bis(1-naphtyl)diazene
• di-α-naphthyldiimide
• AZONAPHTHALENES
• 1,2'-azonaphthalene
• (E)-1,2-Di(1-naphthyl)diazene
• 1,2-Di(1-naphtyl)diazene
• di(naphthalen-1-yl)diazene
• 1,1-AZONAPHTHALENE TECH

1,1'-Azonaphthalene - 80%

CAS: 487-10-5

1,1'-Azonaphthalene is a quinoid that produces an azobenzene with a 1,3-dipolar cycloaddition reaction. This azobenzene is used as a model system for the study of enzyme inducers. It acts as an inhibitor of vascular endothelial growth factor (VEGF) and has been shown to inhibit tumor growth in murine hepatoma models. 1,1'-Azonaphthalene also reacts with dimethyl fumarate to form the dichroic compound with high optical activity. The asymmetric synthesis of 1,1'-azonaphthalene is achieved by using catalytic asymmetric hydrogenation with rhodium on carbon as a catalyst. Reaction mechanism studies have revealed that 1,1'-azonaphthalene can be converted into aromatic hydrocarbons by reacting with aliphatic hydrocarbons.

Formula: C₂₀H₁₄N₂

Purity: Min. 80%

Color and Shape: Powder

Molecular weight: 282.34 g/mol

Ref: 3D-FA70913