Examples of 'solution of compound' in a sentence
Meaning of "solution of compound"
solution of compound - Refers to the process of separating a mixture into its individual components or elements
How to use "solution of compound" in a sentence
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solution of compound
A suitable surfactant can be employed in the solution of compound to aid in processing.
The methanolic solution of Compound I was then transferred to an addition funnel.
A solution of paclitaxel in methanol and a solution of compound VI in methanol was mixed.
To a solution of Compound No.
A couple of drops of the acid solution were added to the solution of compound B.
Seeds are treated with a solution of compound I of the present invention in acetone.
The benzenesulphonic acid solution was added to the stirred solution of Compound A.
The aqueous alkaline solution of compound A may contain an organic solvent miscible with water.
A frozen product can be obtained by freezing an aqueous solution of Compound A and base.
This gave a solution of compound 8 in aqueous NaOH.
The black slurry is filtered through Celite to give a solution of Compound VIII.
The solution obtained is therefore a solution of compound 1 in a solvent or mixture of solvents S2.
Crystals were obtained by slow diffusion of pentane to a THF solution of compound 11.
To this solution is added dropwise a solution of compound 27 in anhydrous dichloromethane.
And the solution of compound XXI can be the tetrahydrofuran solution of base 2.
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A solution of paclitaxel in methanol and a solution of compound I in methanol was mixed together.
A solution of compound 3 and veratryl alcohol was prepared as described above in the General Methods.
The resulting suspension was then transferred into the solution of compound AJ in THF.
Preferably, the NaOH solution of compound 8 was washed with MTBE prior to the cyclization reaction.
According to a another aspect therefore, the invention provides a solution of compound 1 in aqueous acetone.
Concentrating a solution of Compound A in an organic solvent to form slurry ;.
Removal of impurities by extraction to get a solution of compound IX ;.
The addition of the resulting solution of Compound ( I ) ethanolamine salt solution to an acid.
Insoluble residue is removed by filtration under a nitrogen blanket, yielding a hexane solution of compound II.
Anhydrous pyridine is added followed by a solution of compound 28 in anhydrous dichloromethane.
To a solution of compound 26 in anhydrous pyridine is added tosyl chloride.
During this time the temperature of the existing solution of compound 2 is preferably kept constant.
The resulting solution of compound ( 3 ) was used in subsequent reactions without any further purification.
More preferably, the solution is a highly concentrated solution of compound I under reflux while heating.
An aqueous saline solution of compound of the invention was administered intravenously ( i . v. ).
In the combination therapy, pirfenidone was solubilized in a solution of Compound I.
The solution of compound ( 4 ) is immediately used without purification for the subsequent reaction.
For example, it may be prepared by spray drying a solution of compound 1.
Methodology mg / ml stock solution of Compound 10 was made up in water.
The mixture was stirred for 1 hour giving a solution of compound 84.
The stock solution of Compound 7 was 1 mM in distilled water.
Preferably, crystallization is achieved by cooling a hot solution of compound 1.5 in the alkanol.
The solution of compound ( III a ) in dimethyl malonate is added.
The toluene layer is separated and used as a solution of compound ( 1 ) in toluene.
A solution of compound ( 1b ) in a solvent such as DMF is cooled in an ice bath.
This can be prepared by adding NaBH3CN to a solution of compound 3.4 and methanol in acetonitrile.
Thus, a solution of compound 15 in a solvent such as THF is transferred to a high pressure reactor.
Concentrated sulfuric acid ( 2 droplets ) was added to a solution of Compound No.
As a control, used was a solution of Compound ( II ) without any stabilizers.
Moles of nicotinic acid is then added to an aqueous solution of compound 13B.
Additional elution of the final solution of compound ( I ) from step b on chromatographic resin ;.
A solution of compound A-2 having properties shown in Table 2 was obtained.
This solution was added to the DMF solution of compound 18.
The stock solution of Compound 4 was 1 mM in DMSO.
The reaction solution was concentrated to give solution of compound ( 4 . ).
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