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59756-60-4

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Synthesis of β-aminostyrenes
A simple process for the preparation of β-aminostyrenes proceeds from anilines by successively diazotizing, reacting with a vinyl ester, and reacting with a secondary amine without purification of the intermediate products. The compounds are reactive enamines useful in organic synthesis.
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(2008/06/13)

Method of controlling aquatic weeds and algae
A method of reducing the vigor of aquatic weeds and algae makes use of a class of 3-phenyl-4(1H)-pyridones and pyridinethiones. The new compounds are characterized by a methyl group on the nitrogen, and usually bear a 5-substituent chosen from a class which is described herein. The phenyl ring may be substituted. The compounds effectively control aquatic weeds and algae, and kill the plants slowly, so that their decomposition does not deplete oxygen in the treated body of water.
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(2008/06/13)

3-Phenyl-5-substituted-4(1H)-pyridones(thiones)
A class of 3-phenyl-4(1H)-pyridones and pyridinethiones are broad-spectrum herbicides. The new compounds are characterized by a small substituent on the nitrogen, and usually bear a 5-substituent chosen from a class described herein. The phenyl ring may be substituted. The compounds are effective herbicides when applied both before and after the emergence of weeds, and are particularly useful for the control of weeds in cotton and rice cropland.
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(2008/06/13)

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62290-75-9
1-methyl-3-phenyl-5-(3-trifluoromethylphenyl)-4-piperidinone

Chemical Properties

Appearance/Colour :White to light yellow solid
Melting Point: 154-155 ºC
Boiling Point: 444.4 °C at 760 mmHg
Flash Point:222.6 °C
Density: 1.274 g/cm³
Storage Temp.:0-6°C
Vapor Pressure: 4.29E-08mmHg at 25°C
PKA: 1.62±0.10(Predicted)
BRN: 1547990
PSA: 22.00000
LogP: 4.73810

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