Examples of 'benzylamine' in a sentence
Meaning of "benzylamine"
Benzylamine is a chemical compound with applications in various industries like pharmaceuticals and organic synthesis
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- The aromatic primary amine C₆H₅-CH₂-NH₂ or its derivatives
How to use "benzylamine" in a sentence
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benzylamine
The benzylamine reactions were carried out as follows.
Examples of the primary amine include benzylamine.
The benzylamine is removed at this temperature by vacuum distillation.
Especially preferred are ditallowyl benzylamine and ditallowyl allylamine.
Benzylamine is selectively removed in all the solvents systems.
Examples of aromatic amines include benzylamine.
Of benzylamine is added to the filtered product.
Illustrative monofunctional amines include cyclohexylamine and benzylamine.
The crude benzylamine was used without further purification.
Synthesis with benzylamine.
Benzylamine has been scientifically proven to help with weight loss.
Carboxymathyletion and coupling of the benzylamine according to an alternative embodiment.
The enzymes can be differentiated on the basis of their affinities for benzylamine and serotonin.
A catalytic amount of benzylamine can be used in the condensation reaction.
A presently preferred ligand for recovering chymosin is benzylamine or a derivative thereof.
See also
The excess benzylamine was distilled off under reduced pressure.
Fixing of benzylamine.
Condensing the benzylamine with one of an activated carboxylic acid to yield the reagent.
The stripped products were then reacted with benzylamine to form the benzylmaleimide derivative.
Particularly good results have been obtained using an alpha-substituted benzylamine.
After removal of the solvents the desired benzylamine derivative is obtained as a colourless oil.
Reaction with an alkylamine or aralkylamine, such as methylamine or benzylamine in methanol.
In this case benzylamine was used in the Buchwald reaction.
The purified protein retained its CAO activity as determined using benzylamine as the substrate.
The excess benzylamine was removed in the first fractions b . p.
This epoxide intermediate is then treated with benzylamine followed with chloroacetyl chloride.
The structure of the expected product was confirmed vía a test reaction, benzylamine 1 eq.
After cooling, the excess benzylamine was evaporated.
Examples of the amines include diisopropanolamine, diphenylamine, ethanolamine and benzylamine.
Among these, benzylamine and aniline are preferably used.
An example is the reaction of cyclopentadiene with benzylamine to form an aza-norbornene.
Benzylamine had the highest sorption coefficient ; phenol had the lowest.
Intermediate 7 was prepared from benzylamine and terephthalic acid.
As the amount of benzylamine precipitate increases, so does the viscosity of the reaction mixture.
As specific examples of the arylaliphatic amines, representative are, benzylamine and phenylethylamine.
Preferably, the monoamine is benzylamine or hexylamine, with hexylamine being most preferred.
Amine salts include for example trialkylamine, procaine, dibenzylamine and benzylamine salts.
Phenylethylamine is a methylated benzylamine derivative which is chiral ; enantiopure forms are obtained by resolving racemates.
The amine salt may comprise triethylamine salt, benzylamine salt and the like.
Benzylamine hydrochloride crystallises from a mixture of methylene chloride and acetone, and is removed by filtration.
A second hydrogenation in the presence of benzylamine leads to the reductive amination product 8.
He discovered that heating benzaldehyde with formamide does not produce benzylidenediformamide as anticipated, but benzylamine.
Among these gamines, cyclohexylamine and benzylamine are preferable and cyclohexylamine is still preferable.
Examples of the nonash dispersants include those of the succinimide, succinamide, benzylamine and ester types.
Benzylamine derivative or pharmaceutically acceptable acid addition salt thereof, and use thereof for medical purposes.
The amine salts may comprise a triethylamine salt, a benzylamine salt and the like.
Phenethylamine and benzylamine are mainly broken down by MAO-B.
The amine salt described above may include triethylamine salt, benzylamine salt and the like.
During the addition of benzylamine the temperature of the solution did not go above 0°C.
The amine salt described above may include a triethylamine salt, a benzylamine salt and the like.
