70207-46-4

Basic information

• Product Name: 9-Ethyl-9H-carbazole-3,6-dicarboxaldehyde
• Synonyms: 9-Ethyl-9H-carbazole-3,6-dicarboxaldehyde;9-Ethyl-9H-carbazole-3,6-dicarbaldehyde
• CAS NO: 70207-46-4
• Molecular Formula: C₁₆H₁₃NO₂
• Molecular Weight: 251.27992
• Mol File: 70207-46-4.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 9-Ethyl-9H-carbazole-3,6-dicarboxaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 9-Ethyl-9H-carbazole-3,6-dicarboxaldehyde(70207-46-4)
• EPA Substance Registry System: 9-Ethyl-9H-carbazole-3,6-dicarboxaldehyde(70207-46-4)

Safety Data

• Hazardous Substances Data: 70207-46-4(Hazardous Substances Data)

Usage

General Description

9-Ethyl-9H-carbazole-3,6-dicarboxaldehyde is a chemical compound with the molecular formula C16H13NO2. It is a yellow solid that is primarily used in organic synthesis as a building block for the production of various other chemical compounds. It is also known for its potential applications in the field of optoelectronics and materials science due to its unique structural and electronic properties. Additionally, it has been studied for its potential use in fluorescent probes, dye-sensitized solar cells, and organic light-emitting diodes. Overall, 9-Ethyl-9H-carbazole-3,6-dicarboxaldehyde is a versatile and important chemical compound with a wide range of potential applications.

Upstream product

• 86-28-2 N-ethylcarbazole 
• 68-12-2 N,N-dimethyl-formamide 
• 33255-13-9 3,6-dibromo-9-ethyl-9H-carbazole 
• 93-61-8 N-methyl-N-phenylformamide 

Downstream Products

• 70207-47-5 3,6-bis(4-nitrostyryl)-9-ethyl carbazole 
• 118128-81-7 3,6-bisstyryl-N-ethylcarbazole 
• 1384247-89-5 3,6-bis[2-phenyl-2-cyanovinyl]-9-ethyl-9H-carbazole 

Relevant articles and documents

Synthesis and properties of dioxa[3.3](3,6)carbazolophane

Dioxa[3.3](3,6)carbazolophane 1 has been synthesized by the cyclization reaction between 3,6-bis(hydroxymethyl)carbazole and corresponding dibromide. The transannular π-π electronic properties of 1 in solution were examined by absorption and emission spectra. The structure of 1 was confirmed by X-ray crystal analysis.

Synthesis of carbazole-derived ligands and their metal complexes: characterization, thermal, catalytic, and electrochemical features

Abstract: Heading from N-ethylcarbazole, two novel carbazole-derived imine compounds and their copper, cobalt, and nickel complexes have been synthesized. Their open structures have been proposed on the basis of various spectroscopic analyses. All the synthesized compounds have also been examined for their catalytic, thermal, and electronic features. Good or moderate results have been obtained for the catalytic activities of the synthesized complexes. Thermal features showed that the coordination compounds can be used in many organic reactions like oxidation reactions depending on high temperatures. Electronic features of these newly synthesized compounds have also been reported for the first time with this paper. Graphical abstract: [Figure not available: see fulltext.]

The synthesis of trianglimines: On the scope and limitations of the [3 + 3] cyclocondensation reaction between (1R,2R)-diaminocyclohexane and aromatic dicarboxaldehydes

The synthesis of aromatic dicarboxaldehydes, using dilithiation methodology is described along with their reactivity, in the [3 + 3] cyclocondensation reaction, with (1R,2R)-diaminocyclohexane to give trianglimine macrocycles. The scope and limitations of the cyclocondensation reaction are studied and some comments on the properties of the novel macrocycles are made such as their conformation in solution and temperature dependent dynamic NMR behaviour.