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27465-51-6

  • Product Name:4'-Ethylpropiophenone
  • Molecular Formula:C11H14O
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Product Details

Purity:99%

High Purity 4'-Ethylpropiophenone 27465-51-6 In Bulk Supply

27465-51-6 Name

Name

4'-Ethylpropiophenone

Synonym

 1-(4-Ethylphenyl)propanone;1-Propanone,1-(4-ethylphenyl)-;Theethylbenzeneacetone;P-ETHYLPROPIOPHENONE;1-(4-ETHYL-PHENYL)-PROPAN-1-ONE;4'-ETHYLPROPIOPHENONE;4-ETHYLPROPIOPHENONE;4'-ETHYLPROPIOPHENONE 96+%

 

27465-51-6 Chemical & Physical Properties

Boiling point

257.5±19.0 °C at 760 mmHg

Density

1.0±0.1 g/cm3

Molecular Formula

C11H14O

Molecular Weight

162.228

Flash Point

 103.2±16.5 °C

PSA

17.07000

LogP

3.19

Exact Mass

162.104462

Vapour Pressure

0.0±0.5 mmHg at 25°C

Index of Refraction

1.504

High Purity 4'-Ethylpropiophenone 27465-51-6 Usage

4-ethylpropiophenone (EPP), Clear colorless liquid, is An impurity of Eperisone (E565800) as muscle relaxant and analgesic. It is a synthetic chemical that belongs to the class of piperidine hydrochloride.

InChI:InChI=1/C11H14O/c1-3-10-4-6-11(7-5-10)8-9(2)12/h4-7H,3,8H2,1-2H3

27465-51-6 Relevant articles

Selective electrochemical oxidation of aromatic hydrocarbons and preparation of mono/multi-carbonyl compounds

Li, Zhibin,Zhang, Yan,Li, Kuiliang,Zhou, Zhenghong,Zha, Zhenggen,Wang, Zhiyong

, p. 2134 - 2141 (2021/09/29)

The produced carbonyl compounds can be further transformed into α-ketoamides, homoallylic alcohols and oximes in a one-pot reaction. 

Palladium-catalyzed room temperature acylative cross-coupling of activated amides with trialkylboranes

Shi, Weijia,Zou, Gang

, (2018/10/02)

The trialkylboranes generated in situ by hydroboration of olefins with BH3 or 9-BBN performed similarly to those separately prepared, making this protocol more practical.

27465-51-6 Process route

p-(n-propyl)ethylbenzene
20024-90-2

p-(n-propyl)ethylbenzene

1-(4-propylphenyl)ethan-1-one
2932-65-2

1-(4-propylphenyl)ethan-1-one

1-(4-ethylphenyl)-1-propanone
27465-51-6

1-(4-ethylphenyl)-1-propanone

Conditions
Conditions Yield
With pyridine; N-hydroxyphthalimide; tetrabutylammonium tetrafluoroborate; oxygen; In 2,2,2-trifluoroethanol; acetonitrile; at 35 ℃; Overall yield = 65 percent; Electrolysis;
 
triethyl borane
97-94-9

triethyl borane

N-methyl-N-tosyl-p-chlorobenzamide
1445317-56-5

N-methyl-N-tosyl-p-chlorobenzamide

1-(4-ethylphenyl)-1-propanone
27465-51-6

1-(4-ethylphenyl)-1-propanone

Conditions
Conditions Yield
With [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; potassium carbonate; In tetrahydrofuran; tert-butyl methyl ether; at 20 ℃; for 24h; Inert atmosphere; Schlenk technique;
88%

27465-51-6 Upstream products

  • 104037-22-1
    104037-22-1

    [1-(4-ethyl-phenyl)-vinyl]-methyl ether

  • 100-41-4
    100-41-4

    ethylbenzene

  • 79-03-8
    79-03-8

    propionyl chloride

  • 123-62-6
    123-62-6

    propionic acid anhydride

27465-51-6 Downstream products

  • 805951-15-9
    805951-15-9

    α-Amino-4-ethyl-propiophenon

  • 20024-90-2
    20024-90-2

    p-(n-propyl)ethylbenzene

  • 99865-21-1
    99865-21-1

    1-(4-ethylphenyl)propane-1,2-dione

  • 78575-12-9
    78575-12-9

    1-(4-ethyl-phenyl)-propan-1-one oxime

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