478556-66-0

  • Product Name1-[9-Ethyl-6-(2-methylbenzoyl)-9H-carbazol-3-yl]ethanone 1-(O-acetyloxime)
  • Molecular FormulaC26H24N2O3
  • Molecular Weight412.488
  • Purity99%
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Product Details

Quick Details

  • CasNo: 478556-66-0
  • Molecular Formula: C26H24N2O3
  • Purity: 99%

Chemical plants supply high-quality 1-[9-Ethyl-6-(2-methylbenzoyl)-9H-carbazol-3-yl]ethanone 1-(O-acetyloxime) 478556-66-0 in bulk

  • Molecular Formula:C26H24N2O3
  • Molecular Weight:412.488
  • Vapor Pressure:1.73E-11mmHg at 25°C 
  • Refractive Index:1.611 
  • Boiling Point:534.16 °C at 760 mmHg 
  • Flash Point:276.85 °C 
  • PSA:60.66000 
  • Density:1.179 g/cm3 
  • LogP:5.64090 

1-[9-Ethyl-6-(2-methylbenzoyl)-9H-carbazol-3-yl]ethanone 1-(O-acetyloxime)(Cas 478556-66-0) Usage

General Description

1-[9-Ethyl-6-(2-methylbenzoyl)-9H-carbazol-3-yl]ethanone 1-(O-acetyloxime) is a chemical compound that belongs to the carbazole family. It is a ketone with an oxime functional group attached to it. 1-[9-Ethyl-6-(2-methylbenzoyl)-9H-carbazol-3-yl]ethanone 1-(O-acetyloxime) has a complex structure consisting of a carbazole ring with an ethyl and 2-methylbenzoyl substituent. The presence of the oxime functional group signifies that it can potentially act as a chelating agent, forming coordination complexes with metal ions. 1-[9-Ethyl-6-(2-methylbenzoyl)-9H-carbazol-3-yl]ethanone 1-(O-acetyloxime) may have potential applications in organic synthesis, coordination chemistry, and possibly pharmaceutical research. Its precise properties and uses would need to be determined through further experimental study.

InChI:InChI=1/C26H24N2O3/c1-5-28-24-12-10-19(17(3)27-31-18(4)29)14-22(24)23-15-20(11-13-25(23)28)26(30)21-9-7-6-8-16(21)2/h6-15H,5H2,1-4H3

478556-66-0 Relevant articles

Green synthesis method of carbazole oxime ester photoinitiator

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Paragraph 0011; 0032; 0033, (2016/11/24)

The invention discloses a green synthesi...

POLYMERIZABLE COMPOUND, POLYMERIZABLE COMPOSITION, POLYMER, AND OPTICALLY ANISOTROPIC BODY

-

Paragraph 0109, (2014/05/07)

The present invention provides a polymer...

Synthesis of 1-{6-(2-methylbenzoyl)-N-ethylcarbazole- 3-yl}-ethane-1-one oxime O-acetate

Zhao, Liang,Qian, Chao,Gong, Ling,Chen, Xin-Zhi

experimental part, p. 105 - 111 (2012/05/20)

1-{6-(2-Methylbenzoyl)-N-ethylcarbazole-...

478556-66-0 Process route

(6-o-methylbenzoyl-N-ethylcarbazol-3-yl)ethanone oxime

(6-o-methylbenzoyl-N-ethylcarbazol-3-yl)ethanone oxime

acetic acid
64-19-7,77671-22-8

acetic acid

ethanone-1-[9-ethyl-6-(2-methylbenzoyl)-9H-carbazole-3-yl]-1-(O-acetyloxime)
478556-66-0

ethanone-1-[9-ethyl-6-(2-methylbenzoyl)-9H-carbazole-3-yl]-1-(O-acetyloxime)

Conditions
Conditions Yield
With boric acid; In water; chlorobenzene; Solvent; Reflux;
80%
3-acetyl-6-(o-methyl benzoyl)-N-ethylcarbazole
1105615-15-3

3-acetyl-6-(o-methyl benzoyl)-N-ethylcarbazole

sodium acetate
127-09-3

sodium acetate

ethanone-1-[9-ethyl-6-(2-methylbenzoyl)-9H-carbazole-3-yl]-1-(O-acetyloxime)
478556-66-0

ethanone-1-[9-ethyl-6-(2-methylbenzoyl)-9H-carbazole-3-yl]-1-(O-acetyloxime)

Conditions
Conditions Yield
3-acetyl-6-(o-methyl benzoyl)-N-ethylcarbazole; sodium acetate; With hydroxylamine hydrochloride; tetrabutylammomium bromide; In water; 1,2-dichloro-ethane; at 70 ℃; for 7h;
With toluene-4-sulfonic acid; In water; 1,2-dichloro-ethane; for 6h; Reflux;
89.8%

478556-66-0 Upstream products

  • 1105615-15-3
    1105615-15-3

    3-acetyl-6-(o-methyl benzoyl)-N-ethylcarbazole

  • 127-09-3
    127-09-3

    sodium acetate

  • 64-19-7
    64-19-7

    acetic acid

  • 86-28-2
    86-28-2

    N-ethylcarbazole

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