Product
Manufacturer supply high quality 2-(2-chlorophenyl)-1-phenylethan-1-one 57479-60-4 with GMP standards
- Molecular Formula: C14H11 Cl O
- Molecular Weight: 230.694
- Vapor Pressure: 4.34E-05mmHg at 25°C
- Boiling Point: 350.6°Cat760mmHg
- Flash Point: 192.2°C
- PSA： 17.07000
- Density: 1.191g/cm3
- LogP: 3.76540
2-(2-chlorophenyl)-1-phenylethan-1-one(Cas 57479-60-4) Usage
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General Description |
2-(2-chlorophenyl)-1-phenylethan-1-one, also known as Fluorolone, is an organic compound with the molecular formula C14H11ClO. It is a pale yellow solid that is used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. This chemical is a ketone, which means it contains a carbonyl group attached to two hydrocarbon groups. It is also classified as an aryl ketone, as it contains an aryl group (phenyl) bonded to the carbonyl group. 2-(2-chlorophenyl)-1-phenylethan-1-one is a key building block in the production of various pharmaceuticals and is commonly used in the synthesis of anti-inflammatory drugs and other therapeutic agents. |
InChI:InChI=1/C14H11ClO/c15-13-9-5-4-8-12(13)10-14(16)11-6-2-1-3-7-11/h1-9H,10H2
57479-60-4 Relevant articles
Benzylic Aroylation of Toluenes Mediated by a LiN(SiMe3)2/Cs+System
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Chemoselective deprotonative functionali...
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Commercially available cinchona alkaloid...
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Preparation of α-aryl acetophenones from...
Copper-Catalyzed Three-Component Carboboronation of Allenes Using Highly Strained Cyclic Ketimines as Electrophiles
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A diastereoselective copper and NHC-liga...
57479-60-4 Process route
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1-(2-chlorophenyl)-2-oxo-2-phenylethyl acetate
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57479-60-4
1-phenyl-2-(2-chlorophenyl)ethanone
| Conditions | Yield |
|---|---|
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With
tris(bipyridine)ruthenium(II) dichloride hexahydrate; diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; triethylamine;
In
acetonitrile;
at 20 ℃;
for 1h;
Inert atmosphere;
UV-irradiation;
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92%
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1-(2-chlorophenyl)-2-oxo-2-phenylethyl benzoate
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57479-60-4
1-phenyl-2-(2-chlorophenyl)ethanone
| Conditions | Yield |
|---|---|
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With
palladium(II) trifluoroacetate; hydrogen; [(4S)-4-[5-bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphanyl-1,3-benzodioxol-4-yl]-4,5,6,7-tetrahydro-1,3-benzodioxol-5-yl]-bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphane;
In
acetone;
at 35 ℃;
for 24h;
under 22502.3 Torr;
chemoselective reaction;
Glovebox;
Autoclave;
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97%
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1-phenyl-2-o-chlorophenyl-2-chloroethanone
