- CasNo 20795-51-1
- Purity 99%
Manufacturer supply good quality 1-Phenylpentan-3-one 20795-51-1 with stock
- Molecular Formula: C11H14O
- Molecular Weight: 162.232
- Vapor Pressure: 0.034mmHg at 25°C
- Refractive Index: 1.5
- Boiling Point: 242.398 °C at 760 mmHg
- Flash Point: 102.668 °C
- PSA： 17.07000
- Density: 0.961 g/cm3
- LogP: 2.59830
1-Phenylpentan-3-one(Cas 20795-51-1) Usage
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General Description |
1-Phenylpentan-3-one, also known as ethyl phenyl ketone or PPK, is a chemical compound with the molecular formula C11H14O. This organic compound belongs to the ketone functional group and consists of a phenyl group (C6H5) attached to the third carbon of a pentanone chain. It is a pale yellow liquid with a distinct sweet, floral scent and is commonly used as a flavoring agent in the food and beverage industry. Additionally, 1-Phenylpentan-3-one is also utilized as an intermediate in the production of pharmaceuticals, perfumes, and other organic compounds. Its unique chemical properties and versatile applications make it a valuable ingredient in various industrial processes. |
InChI:InChI=1/C11H14O/c1-2-11(12)9-8-10-6-4-3-5-7-10/h3-7H,2,8-9H2,1H3
20795-51-1 Relevant articles
NOVEL METHOD FOR OXIDATION OF SECONDARY ALCOHOLS INTO KETONES WITH MOLECULAR OXIGEN BY USING COBALT(II) COMPLEX CATALYST
Yamada, Tohru,Mukaiyama, Teruaki
, p. 519 - 522 (1989)
The oxidation of secondary alcohols into...
Sulfonium ion-promoted traceless Schmidt reaction of alkyl azides
Ardiansah, Bayu,Kakiuchi, Kiyomi,Morimoto, Tsumoru,Tanimoto, Hiroki,Tomohiro, Takenori
, p. 8738 - 8741 (2021/09/08)
Schmidt reaction by sulfonium ions is de...
Chemoselective reduction of ?,￠-unsaturated carbonyl and carboxylic compounds by hydrogen iodide
Matsumoto, Shoji,Marumoto, Hayato,Akazome, Motohiro,Otani, Yasuhiko,Kaiho, Tatsuo
, p. 590 - 599 (2021/03/29)
The selective reduction of ?,￠-unsaturat...
Cobalt-Catalyzed Asymmetric 1,4-Reduction of β,β-Dialkyl α,β-Unsaturated Esters with PMHS
Lu, Dongpo,Lu, Peng,Lu, Zhan
, p. 4861 - 4864 (2021/09/22)
A cobalt-catalyzed asymmetric reduction ...
Scope and Mechanism of the Redox-Active 1,2-Benzoquinone Enabled Ruthenium-Catalyzed Deaminative α-Alkylation of Ketones with Amines
Kirinde Arachchige, Pandula T.,Handunneththige, Suhashini,Talipov, Marat R.,Kalutharage, Nishantha,Yi, Chae S.
, p. 13962 - 13972 (2021/11/20)
The catalytic system formed in situ from...
20795-51-1 Process route
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-
97-94-9
triethyl borane
-
-
N-methyl-3-phenyl-N-tosylpropanamide
-
-
20795-51-1
1-phenylpentan-3-one
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;
|
95%
|
-
-
708222-26-8
N-(hydrocinnamoyl)-2-methylthioaniline
-
-
925-90-6
ethylmagnesium bromide
-
-
20795-51-1
1-phenylpentan-3-one
-
-
63934-53-2
2-(methylthio)aniline hydrochloride
Conditions
| Conditions | Yield |
|---|---|
|
N-(hydrocinnamoyl)-2-methylthioaniline;
With
2-fluoropyridine; trifluoromethylsulfonic anhydride;
In
dichloromethane;
at 0 ℃;
for 0.5h;
ethylmagnesium bromide;
With
cerium(III) chloride;
In
tetrahydrofuran; dichloromethane;
at -78 ℃;
for 2h;
With
hydrogenchloride;
In
ethyl acetate;
|
91%
87% |
20795-51-1 Upstream products
-
60-29-7
diethyl ether
-
18859-19-3
N,N-diethyl-3-phenylpropanamide
-
925-90-6
ethylmagnesium bromide
-
3152-68-9
1-phenyl-pent-1-en-3-one
20795-51-1 Downstream products
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109245-52-5
1-dimethylamino-2-methyl-5-phenyl-pentan-3-one
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538-68-1
pentylbenzene
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57668-97-0
1-phenyl-pentan-3-one semicarbazone
-
1992-50-3
1-phenylpentan-3-ol
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