Examples of 'dicyclohexylamine' in a sentence
Meaning of "dicyclohexylamine"
dicyclohexylamine (noun) - This phrase refers to a chemical compound that consists of cyclohexylamine molecules. It is commonly used in chemistry and pharmaceutical research
How to use "dicyclohexylamine" in a sentence
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dicyclohexylamine
The most preferred secondary amine is dicyclohexylamine.
The dicyclohexylamine salts crystallize as needles.
Preferred organic bases included dicyclohexylamine and adamantanamine.
Is prepared by neutralization of the corresponding acid with dicyclohexylamine.
The tertiary butylamine and dicyclohexylamine salts of atorvastatin are disclosed.
Examples of the cycloalkylamine include cyclohexylamine and dicyclohexylamine.
Dicyclohexylamine dicyclohexylammonium diethylamine.
This method produces mainly cyclohexylamine with little dicyclohexylamine.
The formed dicyclohexylamine hydrochloride is filtered and the dichloromethane is evaporated.
The crude acid is purified through the formation of its dicyclohexylamine salt.
Two common vapor phase inhibitors are dicyclohexylamine nitrite and cyclohexylamine carbonate.
One preferred group of amines for use in the present invention includes diisopropylamine and dicyclohexylamine.
Conversion of the product to its dicyclohexylamine salt gave the title compound.
The Infrared spectrum of the salt of perindopril with dicyclohexylamine.
The signals of dicyclohexylamine covered those of the aliphatic moiety of the product.
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The organic layer is then washed with several portions of water to remove dicyclohexylamine hydrochloride.
An abundant precipitation of dicyclohexylamine hydrochloride is produced that is filtered with a Buchner funnel.
Other volatile organic impurities for example cyclohexanol, cyclohexylamine, dicyclohexylamine also concentrate in this stream.
After one hour, the dicyclohexylamine salt is filtered and then dried.
The Committee reviewed an extensive collection of toxicological studies m cyclamates, cyclohexylamine and dicyclohexylamine.
The filtrate is treated again with 50 g of dicyclohexylamine and left standing overnight.
The deposited dicyclohexylamine salt was isolated by filtration, and washed with 20 ml of ethyl acetate.
Recrystallizing IIF from toluene eliminates the need for forming a dicyclohexylamine ( DCA ) salt as previously reported.
The dicyclohexylamine ( DCHA ) salt precipitates as the solution is run in.
Salts as claimed in claim 6 wherein B is dicyclohexylamine.
Dicyclohexylmethyl carbonate (INNCN) dicyclohexylamine dicyclohexylammonium diethylamine diethylammonium diftitox INNRG.
The process according to claim 1, wherein the amine is dicyclohexylamine.
A second crop of 724 mg of dicyclohexylamine salt product was obtained from the filtrate.
After distilling of the solvent under reduced pressure, 8.0 g of dicyclohexylamine was added.
Treating the dicyclohexylamine salt of a compound of Formula ( I ) with an acid ;.
The present invention provides in another aspect the dicyclohexylamine salt of a compound of Formula ( I ).
Further, the basic cross-linking accelerator ( C ) is preferably dicyclopentylamine or dicyclohexylamine.
The clear solution was seeded with the dicyclohexylamine salt of the title compound ( 14 g ).
Dicyclohexylamine salt of a compound of Formula ( I ).
This product was dissolved in acetone and dicyclohexylamine was added ( 1 eq ).
Example 4 moles of dicyclohexylamine are reacted with 1 mole 35 % phosphoric acid.
After concentrating the solvent under reduced pressure, 6.0 ml of dicyclohexylamine was added thereto.
A mixture of stearic acid, dicyclohexylamine in the molar ratio 1:1 is prepared.
Dicyclohexylmethyl carbonate (INNCN) dicyclohexylamine.
Cyclamates, cyclohexylamine and dicyclohexylamine were reviewed by the Scientific Committee for Food ( SCF ) in 1985.
The Fmoc-Pro-Lac-OPa was then converted to the dicyclohexylamine ( DCHA ) salt.
Example 19 ( comparative example ), Preparation of the dicyclohexylamine salt of Montelukast from a Montelukast acid with a e . e.
Table 8.3 Ecotoxicological data for dicyclohexylamine.
Two molar equivalents of redistilled dicyclohexylamine ( 913 µL ) were then added.
