93449-42-4

Basic information

• Product Name: 2-Naphthalenol, 1-[(4-methoxyphenyl)azo]-, (E)-
• CAS NO: 93449-42-4
• Molecular Formula: C17H14N2O2
• Molecular Weight: 278.31
• Mol File: 93449-42-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Naphthalenol, 1-[(4-methoxyphenyl)azo]-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Naphthalenol, 1-[(4-methoxyphenyl)azo]-, (E)-(93449-42-4)
• EPA Substance Registry System: 2-Naphthalenol, 1-[(4-methoxyphenyl)azo]-, (E)-(93449-42-4)

Safety Data

• Hazardous Substances Data: 93449-42-4(Hazardous Substances Data)

Upstream product

• 100-17-4 para-methoxynitrobenzene 
• 135-19-3 β-naphthol 
• 104-94-9 4-methoxy-aniline 

Downstream Products

• 104-94-9 4-methoxy-aniline 
• 2834-92-6 1-amino-2-naphthol 
• 93449-61-7 1-[(4-Methoxy-phenyl)-hydrazono]-1H-naphthalen-2-one 

Relevant articles and documents

Exploring flow procedures for diazonium formation

The synthesis of diazonium salts is historically an important transformation extensively utilized in dye manufacture. However the highly reactive nature of the diazonium functionality has additionally led to the development of many new reactions including

Gas-chromatographic studies using glass capillary columns with crown-ether type stationary phases. I β-naphthol-azo-crown ethers and related compounds: Synthesis and properties

Azoderivatives containing residues of benzo-15-crown-5 or benzo-18-crown-6 and 2-naphthol were synthesised in order to be employed as stationary phase in GC studies with glass capillary columns. Analogous azo compounds containing anisole, veratrole and phenyl residues were used for comparison. The compounds were characterised by UV-VIS, NMR and DSC measurements.