4'-Ethylpropiophenone

Basic information

Product Name:4'-Ethylpropiophenone
CasNo.:27465-51-6
Molecular Formula:C₁₁H₁₄O
Molecular Weight:

Physical and Chemical Properties

Purity:99%
Boiling Point:
Packing:
Throughput:

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Product Details

CasNo： 27465-51-6

Molecular Formula： C₁₁H₁₄O

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

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

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

: 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;

: 97-94-9
triethyl borane

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

: 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%