N-Ethylcarbazole

Product Information

Molecular Formula:
C14H13N
Molecular Weight:
195.26
Synonyms
9H-Carbazole, 9-ethyl-; 9-Ethyl-9H-carbazole; Carbazole, 9-ethyl-; NSC 60585
IUPAC Name
9-ethylcarbazole
Canonical SMILES
CCN1C2=CC=CC=C2C3=CC=CC=C31
InChI
InChI=1S/C14H13N/c1-2-15-13-9-5-3-7-11(13)12-8-4-6-10-14(12)15/h3-10H,2H2,1H3
InChI Key
PLAZXGNBGZYJSA-UHFFFAOYSA-N
Boiling Point
190°C
Melting Point
68°C
Flash Point
186 °C
Purity
≥95%
Density
1.06148 g/cm3
Solubility
Soluble in DMSO
Appearance
White to Gray to Brown Powder
Storage
Store at RT
Refractive Index
1.6394

Safety Information

Hazards
H411
Precautionary Statement
P273 - P391 - P501

Computed Properties

XLogP3
3.6
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
1
Exact Mass
195.104799419 g/mol
Monoisotopic Mass
195.104799419 g/mol
Topological Polar Surface Area
4.9Ų
Heavy Atom Count
15
Formal Charge
0
Complexity
203
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
JP-2022040133-A A photosensitive coloring composition for a color filter for a solid-state image sensor, a color filter, and a solid-state image sensor using the same. 2021-12-15
CN-114042453-A Pt-Ce dehydrogenation catalytic material, preparation method and application thereof 2021-12-06
CN-113866044-A Method for testing liquid organic hydrogen storage material 2021-11-23
CN-113926462-A Hydrogenation catalytic material, preparation method and application 2021-11-19
CN-113941303-A Nitration system, synthesis system and method for continuously synthesizing permanent violet 2021-11-02
CN-113856562-A Circulating reaction system for liquid organic matter hydrogenation 2021-10-31
CN-113814395-A Metallic tin reinforced nano TiO2Photocuring 3D printing ceramic slurry and preparation method thereof 2021-10-08
CN-113944589-A Offshore energy comprehensive utilization device system and method based on hydrogen-fired power generation system 2021-10-08
CN-113745547-A Direct liquid organic hydrogen carrier fuel cell based on hydrogen storage alloy electrode 2021-09-07
CN-113851683-A Preparation method of carbazole polyaromatic hydrocarbon piperidine anion exchange membrane 2021-08-27

Literatures

PMID Publication Date Title Journal
22459937 2012-07-01 Synthesis, photophysical and electrochemical properties of a carbazole dimer-based derivative with benzothiazole units Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
21795100 2011-10-15 Experimental and theoretical study of three new benzothiazole-fused carbazole derivatives Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
21953930 2011-10-04 Dehydrogenation of dodecahydro-N-ethylcarbazole on Pd/Al2O3 model catalysts Chemistry (Weinheim an der Bergstrasse, Germany)
22091202 2011-08-01 1,2-Bis[5-(9-ethyl-9H-carbazol-3-yl)-2-methyl-thio-phen-3-yl]-3,3,4,4,5,5-hexa-fluoro-cyclo-pentene Acta crystallographica. Section E, Structure reports online
21338090 2011-03-17 Thermodynamic analysis of strain in the five-membered oxygen and nitrogen heterocyclic compounds The journal of physical chemistry. A
21050099 2011-03-01 Preparatory studies of composite mesenchymal stem cell islets for application in intraportal islet transplantation Upsala journal of medical sciences
21383848 2011-02-23 In vitro dedifferentiation of melanocytes from adult epidermis PloS one
21580339 2010-02-10 9-Ethyl-3,6-bis-(5-iodo-2-thien-yl)-9H-carbazole Acta crystallographica. Section E, Structure reports online
20015681 2010-02-01 Experimental and theoretical study of a new carbazole derivative having terminal benzimidazole rings Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
19908515 2009-10-01 Electropolymerization of N-ethylcarbazole on single walled carbon nanotubes-cyclic voltammetry, raman and FTIR studies Journal of nanoscience and nanotechnology
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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