ਇੱਕ ਰੰਗਹੀਣ ਜਲਣਸ਼ੀਲ ਗੈਸ ਨੂੰ ਕਈ ਵਾਰ ਸਾਹ ਲੈਣ ਵਾਲੀ ਬੇਹੋਸ਼ ਕਰਨ ਲਈ ਵਰਤਿਆ ਜਾਂਦਾ ਹੈ,

cyclopropane's Usage Examples:

Carbene additions to alkenesOne of the most synthetically important cheletropic reactions is the addition of a singlet carbene to an alkene to make a cyclopropane (see figure at left).

1-Aminocyclopropane-1-carboxylic acid (ACC) is a disubstituted cyclic α-amino acid in which a three-membered cyclopropane ring is fused to the Cα atom.

Cyclopropane fatty acids (CPA) are a subgroup of fatty acids that contain a cyclopropane group.

Methylenecyclopropane is an organic compound with the formula (CH2)2CCH2.

5°, which results in angle strain as in the comparable cyclopropane and ethylene oxide molecules.

Molecules with a high amount of ring strain consist of three, four, and some five-membered rings, including: cyclopropanes, cyclopropenes, cyclobutanes, cyclobutenes, [1,1,1]propellanes, [2,2,2]propellanes, epoxides, aziridines, cyclopentenes, and norbornenes.

In enzymology, a cyclopropane-fatty-acyl-phospholipid synthase (EC 2.

Methylcyclopropane is an organic compound with the structural formula C3H5CH3.

Bent bonds are found in strained organic compounds such as cyclopropane, oxirane and aziridine.

Because of the bond's instability, cyclopropane is more reactive than other alkanes.

Strain is most commonly discussed for small rings such as cyclopropanes and cyclobutanes, whose internal angles are substantially smaller than the idealized value of approximately 109°.

rearrangement is an organic reaction for converting a geminal dihalo cyclopropane to an allene using an organolithium base.

Methylcyclopropane, like many other cyclopropanes, undergoes ring-opening reactions.