5599-49-5

Usage

Uses

Used in Dye and Pigment Production:
3-Ethylcarbazole is used as a key component in the production of dyes and pigments, contributing to their color and stability.
Used in Pharmaceutical Industry:
3-Ethylcarbazole serves as an important reactant in the synthesis of various pharmaceuticals, playing a crucial role in the development of new medications.
Used in Organic Synthesis:
As a reactant, 3-ethylcarbazole is utilized in the synthesis of a wide range of organic compounds, showcasing its versatility in chemical reactions.
Used in OLED Technologies:
3-Ethylcarbazole is employed in the development of organic light-emitting diode (OLED) technologies, taking advantage of its light-emitting properties and stability.
Used in Solar Cell Research:
3-ETHYLCARBAZOLE has been studied for its potential application in solar cells, indicating its possible use in the advancement of renewable energy technologies.
Used in Anti-Cancer Research:
3-Ethylcarbazole has been investigated for its potential as an anti-cancer agent due to its cytotoxic properties, which may contribute to the development of new cancer treatments.

InChI:InChI=1/C14H13N/c1-2-10-7-8-14-12(9-10)11-5-3-4-6-13(11)15-14/h3-9,15H,2H2,1H3

Upstream product

• 859805-47-3 6-ethyl-1,2,3,4-tetrahydro-carbazole 
• 3215-37-0 3-acetylcarbazole 
• 5441-51-0 4-ethylcyclohexanone 
• 59-88-1 phenylhydrazine hydrochloride 
• 108-94-1 cyclohexanone 
• 54840-34-5 (4-ethylphenyl)hydrazine 
• 574-39-0 9-acetylcarbazole 

Relevant academic research and scientific papers

Dearomatization-Rearomatization Strategy for Synthesizing Carbazoles with 2,2′-Biphenols and Ammonia by Dual C(Ar)-OH Bond Cleavages

Carbazole is an essential building block in various pharmaceuticals, agrochemicals, natural products, and materials. For future sustainability, it is highly desirable to synthesize carbazole derivatives directly from renewable resources or cheap raw materials. Phenolic compounds are a class of degradation products of lignin. On the other hand, ammonia is a very cheap industrial inorganic chemical. Herein, an efficient dearomatization-rearomatization strategy has been developed to directly cross-couple 2,2′-biphenols with ammonia by dual C(Ar)-OH bond cleavages. This strategy provides a greener pathway to synthesize valuable carbazole derivatives from phenols.

One-pot synthesis of carbazoles from cyclohexanones and arylhydrazine hydrochlorides under metal-free conditions

One-pot synthesis of carbazoles from cyclohexanones and arylhydrazine hydrochlorides is disclosed. Various substituted carbazoles were obtained in moderate to good yields via a sequence of condensation, cyclization and dehydrogenation under metal free conditions using molecular oxygen as an oxidant.

Synthesis of carbazoles from o-cyclohex-2-enylanilines

Several carbazoles (4a-f) have been synthesised from o-cyclohex-2- enylanilines by treatment with pyridine hydrotribromide in methylene chloride at 05 °C for 2 h followed by refluxing with Pd-C in diphenyl ether for 1 h.