Examples of 'trifluoroethanol' in a sentence
Meaning of "trifluoroethanol"
trifluoroethanol (noun) - Trifluoroethanol is a type of organic compound with a distinct chemical structure. It is often used in scientific contexts, such as chemistry or biochemistry, for research or experimental purposes
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- Any of several isomers of an alcohol formally derived from ethanol by replacing three hydrogen atoms by those of fluorine, but especially 2,2,2-trifluoroethanol
How to use "trifluoroethanol" in a sentence
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trifluoroethanol
Oxidation of trifluoroethanol yields trifluoroacetaldehyde or trifluoroacetic acid.
Process for the preparation of trifluoroethanol.
One mole of trifluoroethanol was allowed to flow in slowly.
This species was prepared by the reaction of trifluoroethanol with acetylene.
Trifluoroethanol is used as a solvent in organic chemistry.
Fluoroalcholos such as trifluoroethanol can also be used.
The trifluoroethanol was evaporated on a rotary evaporator.
The present invention relates to a process for the preparation of trifluoroethanol.
The unreacted trifluoroethanol was evaporated off.
As a labelling reagent for the carboxyl groups, trifluoroethanol is used.
Trifluoroethanol is used as a synthetic intermediate in the pharmaceutical and plant protection industries.
The invention is particularly advantageous for obtaining trifluoroethanol by hydrogenation of trifluoroacetic acid.
Trifluoroethanol is an oxidation-resistant polar solvent.
The invention is particularly indicated for the preparation of trifluoroethanol by hydrogenation of trifluoroethyl trifluoroacetate.
Trifluoroethanol is extremely acidic, much more acidic than ethanol.
See also
It is often confused with Ethanol because Trifluoroethanol smells similar to Ethanol.
The trifluoroethanol results are shown in Table 3.
This material was suspended in 25 mL trifluoroethanol and was heated to reflux.
Trifluoroethanol was substantially removed in a rotary evaporator after adding water ( 20 mL ).
A process for the preparation of trifluoroethanol by hydrolysis, in the gas phase, of chlorotrifluoroethane.
To the solution was added 50g of trifluoroethanol.
Trifluoroethanol is the organic compound with the formula CF3CH2OH.
The process according to claim 13 wherein the solvent is trifluoroethanol.
The solid was then suspended in 15 mL trifluoroethanol and heated to reflux for 2h.
FIG . 3 the circular dichroism spectra of pentagastrin-histamine, pentagastrin and aminosuccinyl pentagastrin, in trifluoroethanol.
Peptides were dissolved in trifluoroethanol ( TFE ) and mixed with soy phosphatidylcholine ( PC ) in chloroform.
Figure 62 is an FT-Raman spectrum for carvedilol hydrobromide trifluoroethanol solvate.
Trifluoroethanol ( " TFE " ) is the preferred fluorinated alcohol.
Figure 110 is an x-ray powder diffractogram for carvedilol hydrobromide trifluoroethanol solvate.
Ml of dimethylformamide and 36 ml ( 475 mmol ) of trifluoroethanol are introduced into this round bottom flask.
Preferably the capping group reagent is a hydroxyhaloalkyl compound, preferably a C1-12 hydroxyhaloalkyl compound, preferably trifluoroethanol.
Peptides were dissolved in trifluoroethanol ( TFE ).
Trifluoroethanol ( TFE ), an inducer of alpha-helical conformation was added, and the spectra were recorded.
Figure 65 is an FT-IR spectrum for carvedilol hydrobromide trifluoroethanol solvate.
The alcohols used were trifluoroethanol ( TFE ) and hexafluoroisopropanol ( HFIP ).
Figure 2 shows CD spectra of peptides and antioxidant peptides in trifluoroethanol ( TFE ) and water.
Some of the samples contained trifluoroethanol ( TFE ) ( expressed as % vol ).
G of 4-carboxy thiazolidine are dissolved in 20 ml of trifluoroethanol.
Afterwards, the reaction mixture was concentrated, then trifluoroethanol ( 10 mL ) was added.
The resulting degree of conversion of the trifluoroethyl trifluoroacetate was 97 % and the trifluoroethanol yield was 96 %.
The resulting degree of conversion of the ethyl trifluoroacetate was 30 % and the trifluoroethanol yield was 97 %.
The resulting degree of conversion of the phenyl trifluoroacetate was 100 % and the trifluoroethanol yield was 98 %.
