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1-methylprop-1-enylcyclopropane

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Identification
Molecular formula
C7H12
CAS number
1647-53-4
IUPAC name
1-methylprop-1-enylcyclopropane
State
State

At room temperature, 1-methylprop-1-enylcyclopropane is in a liquid state.

Melting point (Celsius)
-80.00
Melting point (Kelvin)
193.15
Boiling point (Celsius)
103.00
Boiling point (Kelvin)
376.15
General information
Molecular weight
96.17g/mol
Molar mass
96.1700g/mol
Density
0.6900g/cm3
Appearence

1-Methylprop-1-enylcyclopropane is a colorless liquid. It is typically clear and free from any visible impurities when pure.

Comment on solubility

Solubility of 1-methylprop-1-enylcyclopropane

1-methylprop-1-enylcyclopropane, a compound with a complex structure, exhibits noteworthy characteristics regarding its solubility. Generally, its solubility can be influenced by several factors such as:

  • Molecular Structure: The presence of cyclopropane within its structure can affect interaction with solvents.
  • Polarity: Due to its hydrocarbon nature, 1-methylprop-1-enylcyclopropane is mostly nonpolar, making it less soluble in polar solvents like water.
  • Solvent Compatibility: This compound tends to be more soluble in nonpolar solvents such as hexane or heptane.

As a rule of thumb, "like dissolves like" plays a crucial role here, meaning:

  • It will readily dissolve in organic solvents.
  • It will have minimal solubility in aqueous environments.

In practical terms, if you want to use 1-methylprop-1-enylcyclopropane for applications, it is important to consider the solvent in which it will be employed. For best results, utilize solvents that match its nonpolar characteristics effectively.

Interesting facts

Interesting Facts about 1-Methylprop-1-enylcyclopropane

1-Methylprop-1-enylcyclopropane is a fascinating compound within the realm of organic chemistry. As a member of the cyclopropane family, it exhibits unique properties and applications that make it stand out.

Structural Characteristics

  • Cyclopropane Ring: The cyclopropane ring structure is known for its high angle strain due to its three-membered carbon framework.
  • Alkene Substitution: Being an alkene, the presence of the double bond contributes to its reactivity, allowing for various chemical transformations.

Reactivity and Applications

This compound is not just a theoretical construct; its reactivity opens up numerous pathways for synthetic chemists. Here are some notable applications:

  • Building Block: It serves as a key building block in synthesizing more complex organic molecules.
  • Flavors and Fragrances: Similar compounds are often used in the manufacture of certain flavors and fragrances, showcasing their importance in industrial applications.

Scientific Significance

From a scientific viewpoint, 1-methylprop-1-enylcyclopropane is intriguing because:

  • It contributes to the study of ring strain and its effects on reactivity.
  • Research on this compound aids in understanding the behavior of alkenes in various chemical reactions, furthering the field of organic synthesis.

Quote: "Understanding compounds like 1-methylprop-1-enylcyclopropane expands our horizons in synthetic chemistry, pushing the boundaries of what we can create."

In conclusion, 1-methylprop-1-enylcyclopropane, with its unique structural and chemical properties, not only serves as a valuable compound in research and industry but also ignites curiosity and inspires innovation in the field of chemistry.

Synonyms
SCHEMBL4834078
SCHEMBL16287798
(1-methyl-1-propenyl)cyclopropane