1484-04-4

  • Product Name:1-(9-Ethyl-9H-carbazol-3-yl)ethan-1-one
  • Molecular Formula:C16H15NO
  • Purity:99%
  • Molecular Weight:237.301
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Product Details;

CasNo: 1484-04-4

Molecular Formula: C16H15NO

factory and supplier 1484-04-4 1-(9-Ethyl-9H-carbazol-3-yl)ethan-1-one in stock

  • Molecular Formula:C16H15NO
  • Molecular Weight:237.301
  • Vapor Pressure:3.58E-05mmHg at 25°C 
  • Melting Point:115 °C 
  • Boiling Point:353.5oC at 760 mmHg 
  • Flash Point:167.6oC 
  • PSA:22.00000 
  • Density:1.12g/cm3 
  • LogP:4.01700 

1-(9-ETHYL-9H-CARBAZOL-3-YL)ETHANONE(Cas 1484-04-4) Usage

General Description

1-(9-Ethyl-9H-carbazol-3-yl)ethanone, also known as Ethylcarbazole ketone, is a chemical compound with the molecular formula C17H15NO. It is a ketone derivative of carbazole, which is a heterocyclic aromatic organic compound. Ethylcarbazole ketone is widely used as a reactant in organic synthesis and as an intermediate in the production of various pharmaceuticals, agrochemicals, and dyes. It has also been studied for its potential applications in the development of organic electronic materials and optoelectronic devices. Additionally, it possesses antioxidant and anti-inflammatory properties, making it a potential candidate for the development of new drugs. 1-(9-ETHYL-9H-CARBAZOL-3-YL)ETHANONE should be handled and used with care, following proper safety precautions and guidelines for handling hazardous chemicals.

InChI:InChI=1/C16H15NO/c1-3-17-15-7-5-4-6-13(15)14-10-12(11(2)18)8-9-16(14)17/h4-10H,3H2,1-2H3

1484-04-4 Relevant articles

A short route to heteroarylcarbazoles: Synthesis of new pyrazolylcarbazoles and carbazolylquinolines

Nagarajan, Rajagopal,Perumal, Paramasivan T.

, p. 1269 - 1273 (2004)

A short synthesis of pyrazolylcarbazoles...

Facile procedure for the synthesis of 3-acetyl-9-ethylcarbazole and corresponding functionalized bis-diketone compounds

Tang, Rui-Ren,Zhang, Wei

, p. 601 - 606 (2010)

Acetylation-substituted N-ethylcarbazole...

A New and Facile Method for the Synthesis of Nitrocarbazoles by Urea Nitrate

Nagarajan, Rajagopal,Muralidharan,Perumal, Paramasivan T.

, p. 1259 - 1264 (2004)

Urea nitrate in acetic acid is found to ...

Pure Organic Room Temperature Phosphorescence from Excited Dimers in Self-Assembled Nanoparticles under Visible and Near-Infrared Irradiation in Water

Wang, Xiao-Fang,Xiao, Hongyan,Chen, Peng-Zhong,Yang, Qing-Zheng,Chen, Bin,Tung, Chen-Ho,Chen, Yu-Zhe,Wu, Li-Zhu

, p. 5045 - 5050 (2019)

Pure organic room temperature phosphores...

A facile method for the synthesis of acetylcarbazoles and carbazole aldehydes

Nagarajan, Rajagopal,Perumal, Paramasivan T.

, p. 2127 - 2133 (2004)

Acetylation of 9-alkylcarbazoles with ac...

HS? facilitated sulfur pyran realizing hydrogen sulfide detection and imaging in HepG2 cells and chlorella

Chao, Jianbin,Xu, Miao,Zhang, Yongbin,Huo, Fangjun,Liu, Yaoming,Wang, Xiaolu,Yin, Caixia

, p. 227 - 232 (2019)

The new carbazole-based fluorescent prob...

Influence of thiophene spacer and auxiliary acceptor on the optical properties of 4-(Diethylamino)-2-hydroxybenzaldehyde based D-π-A-π-D Colorants with N-alkyl donors: Experimental, DFT and Z-scan study

Raikwar, Manish M.,Patil, Dinesh S.,Mathew, Elizabeth,Varghese, Manu,Joe, Issac H.,Sekar, Nagaiyan

, p. 45 - 58 (2019)

We report here design and synthesis of f...

A Solid-State Fluorescent Material Based on Carbazole-Containing Difluoroboron β-Diketonate: Multiple Chromisms, the Self-Assembly Behavior, and Optical Waveguides

Chen, Peng-Zhong,Zhang, Han,Niu, Li-Ya,Zhang, Yi,Chen, Yu-Zhe,Fu, Hong-Bing,Yang, Qing-Zheng

, (2017)

A carbazole-containing difluoroboron β-d...

Fluorescent probe of reversible sulfur dioxide/sulphurous acid (hydrogen) salt

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Paragraph 0025; 0026, (2018/06/16)

The invention provides a fluorescent pro...

1484-04-4 Process route

N-ethylcarbazole
86-28-2

N-ethylcarbazole

acetic anhydride
108-24-7

acetic anhydride

N-ethyl-3-acetylcarbazole
1484-04-4

N-ethyl-3-acetylcarbazole

Conditions
Conditions Yield
N-ethylcarbazole; acetic anhydride; With boron trifluoride diethyl etherate; at 20 ℃; for 4h;
With hydrogenchloride; water;
80.4%
With aluminum (III) chloride; In dichloromethane; at 0 - 20 ℃;
70%
With aluminum (III) chloride; In dichloromethane; at 20 ℃; for 4h;
70.47%
With perchloric acid; triphenylphosphine; In dichloromethane; at 20 ℃; for 2h;
61%
With bismuth(III) chloride; In dichloromethane; at 20 ℃; for 0.583333h;
60%
With In(OSO2CF3)3; In dichloromethane; for 2.5h;
59%
N-ethylcarbazole; With aluminum (III) chloride; In dichloromethane; at 20 ℃; for 0.5h;
acetic anhydride; In dichloromethane; at 0 - 20 ℃; for 6h;
N-ethylcarbazole
86-28-2

N-ethylcarbazole

acetyl chloride
75-36-5

acetyl chloride

N-ethyl-3-acetylcarbazole
1484-04-4

N-ethyl-3-acetylcarbazole

Conditions
Conditions Yield
With bismuth(III) chloride; In dichloromethane; at 20 ℃;
81%
With zinc(II) chloride; In dichloromethane; at 20 ℃; for 6h;
80%
With zinc(II) chloride;
With zinc(II) chloride; In dichloromethane; at 20 ℃; for 24h;
With aluminum (III) chloride; In dichloromethane; at 20 ℃; for 4h; Cooling with ice;
With zinc(II) chloride; In dichloromethane; for 5h; Reflux;
With aluminum (III) chloride; In dichloromethane;

1484-04-4 Upstream products

  • 86-28-2
    86-28-2

    N-ethylcarbazole

  • 75-36-5
    75-36-5

    acetyl chloride

  • 108-24-7
    108-24-7

    acetic anhydride

  • 86-74-8
    86-74-8

    9H-carbazole

1484-04-4 Downstream products

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    1219036-84-6

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    1239875-14-9

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