Home >Pharmaceutical > 4-Phenylcyclohexanone
- Chemical Name: 4-Phenylcyclohexanone
- CAS No.: 4894-75-1
Quality Factory Hot Selling 4-Phenylcyclohexanone 4894-75-1 with Fast Shipping
- Molecular Formula: C12H14O
- Molecular Weight: 174.243
- Appearance/Colour: white to off-white crystalline powder
- Vapor Pressure: 0.00167mmHg at 25°C
- Melting Point: 73-77 °C(lit.)
- Refractive Index: 1.537
- Boiling Point: 294 °C at 760 mmHg
- Flash Point: 123.7 °C
- PSA： 17.07000
- Density: 1.042 g/cm3
- LogP: 2.91330
4-Phenylcyclohexanone(Cas 4894-75-1) Usage
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General Description |
4-Phenylcyclohexanone undergoes Ruthenium-catalyzed reaction with tributylamine to yield 2-butyl-4-phenylcyclohexanone and 2,6-dibutyl-4-phenylcyclohexanone. Wittig reaction of 4-phenylcyclohexanone with (carbethoxymethylene)triphenylphosphorane under microwave irradiation has been investigated. |
InChI:InChI=1/C12H14O/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-5,11H,6-9H2
4894-75-1 Relevant articles
Merging Halogen-Atom Transfer (XAT) and Copper Catalysis for the Modular Suzuki-Miyaura-Type Cross-Coupling of Alkyl Iodides and Organoborons
Zhang, Zhenhua,Górski, Bartosz,Leonori, Daniele
, p. 1986 - 1992 (2022/02/01)
We report here a mechanistically distinc...
Electrochemically Enabled, Nickel-Catalyzed Dehydroxylative Cross-Coupling of Alcohols with Aryl Halides
Li, Zijian,Sun, Wenxuan,Wang, Xianxu,Li, Luyang,Zhang, Yong,Li, Chao
supporting information, p. 3536 - 3543 (2021/03/08)
As alcohols are ubiquitous throughout ch...
Ground-State Electron Transfer as an Initiation Mechanism for Biocatalytic C-C Bond Forming Reactions
Fu, Haigen,Lam, Heather,Emmanuel, Megan A.,Kim, Ji Hye,Sandoval, Braddock A.,Hyster, Todd K.
, p. 9622 - 9629 (2021/07/01)
The development of non-natural reaction ...
Deciphering Reactivity and Selectivity Patterns in Aliphatic C-H Bond Oxygenation of Cyclopentane and Cyclohexane Derivatives
Martin, Teo,Galeotti, Marco,Salamone, Michela,Liu, Fengjiao,Yu, Yanmin,Duan, Meng,Houk,Bietti, Massimo
supporting information, p. 9925 - 9937 (2021/06/30)
A kinetic, product, and computational st...
4894-75-1 Process route
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![(+/-)-5-phenylbicyclo[3.1.0]hexan-2-one](/upload/2026/5/77e1d39363844b2b97055144831ef54a_c18943ea-c4da-45fb-9ab9-d165bcdc5788.png)
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(+/-)-5-phenylbicyclo[3.1.0]hexan-2-one
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4894-75-1
1-phenyl-4-cyclohexanone
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5769-13-1,7335-12-8,5437-46-7
4-phenyl-cyclohexanol
| Conditions | Yield |
|---|---|
|
With
lithium; tert-butyl alcohol;
In
diethyl ether; ammonia;
for 0.25h;
Heating;
|
44%
35% |
-
-
87143-17-7
4-phenyl-1-methylenecyclohexane
-
-
4894-75-1
1-phenyl-4-cyclohexanone
| Conditions | Yield |
|---|---|
|
With
2,6-dimethylpyridine; sodium periodate; ruthenium(III) chloride trihydrate;
In
dichloromethane; water; acetonitrile;
at 20 ℃;
for 1h;
Inert atmosphere;
|
87%
|
4894-75-1 Upstream products
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930-68-7
cyclohexenone
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25163-93-3
8-phenyl-1,4-dioxaspiro[4,5]decane
-
5437-46-7
trans-4-phenylcyclohexanol
-
827-52-1
1-phenyl-1-cyclohexane
4894-75-1 Downstream products
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67688-28-2
4-phenylcycloheptanone
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1079-68-1
(+/-)-trans -2-bromo-4-phenyl-cyclohexanone
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109337-60-2
4-phenylcyclohexan-1-d-1-ol
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102162-15-2
1-(2-Methoxy-phenyl)-4-phenyl-cyclohexanol