Examples of 'cyclohexylamine' in a sentence
Meaning of "cyclohexylamine"
Cyclohexylamine is a chemical compound used as an intermediate in the synthesis of pharmaceuticals and other organic compounds
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- The primary amine derived from cyclohexane by replacing a hydrogen atom by an amino group; any derivative of this compound
How to use "cyclohexylamine" in a sentence
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cyclohexylamine
Amine q may also be cyclohexylamine or other cycloalkylamine.
The herbicide hexazinone is derived from cyclohexylamine.
A monoamine such as cyclohexylamine is therefore no longer necessary as a terminator.
Particularly preferred amines are methylamine and cyclohexylamine.
This method produces mainly cyclohexylamine with little dicyclohexylamine.
Examples of cycloalkylamino include cyclopropylamino and cyclohexylamine.
Cyclohexylamine is the preferred cycloalkylamine.
Examples of the cycloalkylamine include cyclohexylamine and dicyclohexylamine.
The use of cyclohexylamine as a boiler water additive in food processing facilities.
Illustrative monofunctional amines include cyclohexylamine and benzylamine.
Sodium cyclamate and cyclohexylamine may be found in products available to consumers.
The combination comprises a phenylenediamine and cyclohexylamine compound or derivative.
Uncomplexed cyclohexylamine is not stable during the heating of the adhesive.
Concentration of the filtrate gave additional cyclohexylamine hydrochloride mixed with an oil.
Cyclohexylamine is usually converted with the help of amido sulphonic acid.
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The hydrogenolysis of a series of alkylcesiums in cyclohexylamine solvent has been studied spectrophotometrically.
The herbicide hexazinone and the anesthetic hexylcaine are derived from cyclohexylamine.
Two common vapor phase inhibitors are dicyclohexylamine nitrite and cyclohexylamine carbonate.
Cyclohexylamine and cyclohexyldimethylamine, and their salts.
This can be accomplished by reacting cyclohexylamine with either sulfamic acid or sulfur trioxide.
Cyclohexylamine is an organic compound, belonging to the aliphatic amine class.
The complex of cyclodextrin and cyclohexylamine stabilizes the cyclohexylamine during the heating process.
Stirring was continued for two hours at room temperature until the cyclohexylamine salt precipitated.
An important cyclohexylamine is sertralin,.
Preferred are the sulfenamides from isopropylamine, t-butylamine and cyclohexylamine.
Particularly preferred are cyclohexylamine and n-hexylamines.
New cyclohexylamine derivatives having beta2 adrenergic agonist and m3 muscarinic antagonist activities.
To supplement the data basis, the related substance cyclohexylamine is reviewed.
An important cyclohexylamine is sertraline,.
This compound is synthesized by the method of Example 1, starting with cyclohexylamine.
Among these gamines, cyclohexylamine and benzylamine are preferable and cyclohexylamine is still preferable.
The Committee reviewed an extensive collection of toxicological studies m cyclamates, cyclohexylamine and dicyclohexylamine.
The waxes may be melted, and the cyclohexylamine compound is dispersed homogeneously therein by stirring.
Figure 6 shows the X-ray powder diffraction pattern of the cyclohexylamine salt of Montelukast.
In a similar manner, cyclohexylamine may be substituted for n - octylamine to afford 3-cyclohexylisothiazolone.
This leaves approximately 63 % for conversion to cyclohexylamine by intestinal flora.
Then, 6.5 ml of cyclohexylamine was added and the mixture was agitated at the room temperature.
In other aspects, the different base used is cyclohexylamine to form the cyclohexylammonium salt.
Cyclohexylamine was added until the pH was approx . 10, then methanol was added until a turbidity persisted.
It may be prepared by the reaction of cyclohexylamine and S, S-dimethyl dithiocarbonate.
The preferred compounds are butylamine, hexylamine, octylamine, decylamine, laurylamine, stearylamine, cyclohexylamine and aniline.
These precursors are triethyleneamine or TEA, cyclohexylamine or CHA and ethylenediamine or EDA.
Suitable dilutants include, but are not limited to water, low molecular weight alcohols, and cyclohexylamine.
Cyclohexylamine is listed as an extremely hazardous substance as defined by Section 302 of the U. S.
Illustrative monofunctional amines include n-nonylamine, isononylamine, stearylamine, cyclohexylamine and benzylamine.
N-cyclohexylsulfamate, N-cyclohexylsulphamate cyclohexylsulfamate (INNCN) cyclohexylamine cyclohexylammonium cyclohexylpropionate cyclohexanepropionate cyclohexylpropanoate daloxate INNRG.
The procedure of Example 1, was repeated, except that methylamine was employed instead of cyclohexylamine.
A selectivity in cyclohexanone oxime equal to 44 % and a cyclohexylamine conversion of 81 % were obtained.
EXAMPLE 14 This example was prepared as described in EXAMPLE 8E, substituting phenethylamine for cyclohexylamine.
The cyclohexylamine salt was isolated by filtration and washed with hexane ( 50 ml ).
