5599-49-5 Usage
General Description
3-ethylcarbazole is a chemical compound that belongs to the carbazole family. It is a pale yellow to light brown solid with a strong odor, and is insoluble in water but soluble in organic solvents. 3-ethylcarbazole is primarily used in the production of dyes, pigments, and pharmaceuticals. It is also used as a reactant in the synthesis of various organic compounds. 3-ETHYLCARBAZOLE has potential applications in OLED (organic light-emitting diode) technologies, as it exhibits high thermal and chemical stability, as well as good light-emitting properties. Additionally, 3-ethylcarbazole has been studied for its potential use in solar cells and as an anti-cancer agent due to its cytotoxic properties. Overall, 3-ethylcarbazole is a versatile compound with a range of industrial and research applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5599-49-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,9 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5599-49:
(6*5)+(5*5)+(4*9)+(3*9)+(2*4)+(1*9)=135
135 % 10 = 5
So 5599-49-5 is a valid CAS Registry Number.
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
5599-49-5Relevant articles and documents
Dearomatization-Rearomatization Strategy for Synthesizing Carbazoles with 2,2′-Biphenols and Ammonia by Dual C(Ar)-OH Bond Cleavages
Cao, Dawei,Yu, Jing,Zeng, Huiying,Li, Chao-Jun
, p. 13200 - 13205 (2020/12/18)
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.
Synthesis of carbazoles from o-cyclohex-2-enylanilines
Majumdar,Das,Kundu
, p. 1593 - 1600 (2007/10/03)
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.
