87353-56-8

Basic information

• Product Name: 3,6-Dichloro-9-(ethoxy-phenyl-methyl)-9H-carbazole
• Synonyms: 3,6-Dichloro-9-(ethoxy-phenyl-methyl)-9H-carbazole
• CAS NO: 87353-56-8
• Molecular Weight: 370.278
• Mol File: 87353-56-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,6-Dichloro-9-(ethoxy-phenyl-methyl)-9H-carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3,6-Dichloro-9-(ethoxy-phenyl-methyl)-9H-carbazole(87353-56-8)
• EPA Substance Registry System: 3,6-Dichloro-9-(ethoxy-phenyl-methyl)-9H-carbazole(87353-56-8)

Safety Data

• Hazardous Substances Data: 87353-56-8(Hazardous Substances Data)

Upstream product

• 5599-71-3 3,6-dichloro-9H-carbazole 
• 64-17-5 ethanol 
• 100-52-7 benzaldehyde 

Downstream Products

• 100-52-7 benzaldehyde 

Relevant articles and documents

N-(α-ALKOXYALKYL)AMINES. SYNTHESIS OF 9-CARBAZOLYLETHOXYPHENYLMETHANES AND THE MECHANISM OF THEIR ACID HYDROLYSIS

It was shown that the acid-catalyzed reaction of benzaldehydes with carbazoles in the presence of ethanol and ethyl orthoformate leads to the formation of 9-carbazolylethoxyphenylmethanes and not acetals or aminals.The kinetics of the acid hydrolysis of the synthesized compounds were studied, and the effect of substituents in the benzene and carbazole rings on the hydrolysis rate was assessed.In conjunction with data on the kinetic isotope effect of the solvent and the entropies of activation, the results are interpreted in terms of a mechanism close to the A-1 mechanism of hydrolysis of acetals with preferential cleavage of the C-O bond and the intermediate formation of a carbenium-immonium ion.