1,1,2,2-Tetramethylcyclopropane is a cyclic hydrocarbon characterized by its unique structure, which consists of a cyclopropane ring with four methyl groups attached to it. This compound is notable for its high degree of steric hindrance due to the bulky methyl groups, which can influence its reactivity and stability. It is a colorless liquid at room temperature and is relatively non-polar, making it less soluble in water but soluble in organic solvents. The presence of multiple methyl groups contributes to its relatively high boiling point compared to other cyclopropane derivatives. Additionally, 1,1,2,2-tetramethylcyclopropane is known for its low reactivity under standard conditions, which makes it a stable compound. It is primarily used in organic synthesis and as a reference compound in various chemical studies. Its unique structure and properties make it of interest in the fields of organic chemistry and materials science.

1,1,2,2-Tetramethylcyclopropane

4127-47-3: Cyclopropane, 1,1,2,2-tetramethyl-, 1,1,2,2-Tetramethylcyclopropane

1,1,2,2-Tetramethylcyclopropane is a methyl derivative of cyclopropane. The chemical nature of the compound has not been fully elucidated yet. It was postulated that 1,1,2,2-Tetramethylcyclopropane undergoes ring-opening to form methyl radicals and methane monooxygenase as the reaction mechanism. The activation energy for this reaction was found to be 76 kJ/mol at room temperature. The product of this chemical reaction is methane monooxygenase. 1,1,2,2-Tetramethylcyclopropane can be used in reactions where the substrate concentration is low or when high temperatures are required.

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CAS 4127-47-3: 1,1,2,2-Tetramethylcyclopropane

1,1,2,2-Tetramethylcyclopropane

Ref: 3B-T1721

1,1,2,2-Tetramethylcyclopropane

Ref: 3D-FT75914

1,1,2,2-Tetramethylcyclopropane, 99%

Ref: 02-B20809

1,1,2,2-TETRAMETHYLCYCLOPROPANE

Ref: IN-DA003D65