cyclopropane


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cyclopropane

 [si″klo-pro´pān]
a colorless, flammable gas with a characteristic odor and pungent taste that is an inhalational anesthetic; now little used because of its flammability.

cy·clo·pro·pane

(sī'klō-prō'pān),
An explosive gas of characteristic odor; in the past, widely used to produce general anesthesia.
Synonym(s): trimethylene

cyclopropane

(sī′klə-prō′pān′)
n.
A highly flammable, explosive, colorless gaseous cycloalkane, C3H6, sometimes used as an anesthetic.

cyclopropane

A powerful, non-irritating anaesthetic gas. It has the disadvantages of being explosive and of causing heart irregularity in the presence of adrenaline.
References in periodicals archive ?
Zhao, Synthesis and Antifungal Activity of 1,2,4-triazole Derivatives Containing Cyclopropane Moiety, Lett.
Generally, the average bond angles, bond lengths of phenyl, cyclopropane, and 1,2,4-triazole are within normal ranges [14-19].
Initially several members of the research staff were safely anaesthetised with cyclopropane and a demonstration was arranged for the anaesthetic department.
In view of these facts mentioned above, and also as a part of our work on the synthesis of bioactive lead compounds for drug discover, the title compound was designed by introducing cyclopropane pharmacophore into 1,2,4-triazole scaffold.
Keywords: Thiazole, Cyclopropane, Theoretical calculation, Synthesis, Crystal structure.
The structural characterization of complexes formed by acetylene, ethylene and cyclopropane became known by the hydrogen fluoride as proton donor [103].
Some of the most dynamic bioactive compound observed during spectral studies were a-Amyrin and Cyclopropane carboxamide despite its small proportion in the crude extract.
In the case of cyclopropane fatty acids, we obtained its separation in cheese fat by using apolar capillary column [6]; however, this column is not suitable for the optimal separation of fatty acids, so it is possible that changing the food matrix interferences occur.
In addition, the mutual orientation of the isopropyl substituents and the cyclopropane ring in the bicyclic lactone 9 being formed depend stereospecifically on the mutual orientation of the substituents X and R in the tetrahydropyranyl ring.
Insecticide activity of the pyrethrins and related compounds essential features of insecticide activity in chryseinthemates and related cyclopropane esters.