Skip to main content

Norcarane

ADVERTISEMENT
Identification
Molecular formula
C7H14
CAS number
286-08-8
IUPAC name
norcarane
State
State

At room temperature, norcarane exists as a liquid. It is stable under standard conditions of temperature and pressure.

Melting point (Celsius)
-60.50
Melting point (Kelvin)
212.65
Boiling point (Celsius)
117.70
Boiling point (Kelvin)
390.85
General information
Molecular weight
98.19g/mol
Molar mass
98.1860g/mol
Density
0.8870g/cm3
Appearence

Norcarane is a colorless liquid in its pure form. It is relatively volatile and has a faint, gasoline-like odor.

Comment on solubility

Solubility of Norcarane

Norcarane, with its chemical structure influenced by the distinctive bicyclic arrangement, exhibits intriguing solubility characteristics. Being a hydrocarbon, its solubility in various solvents can be summarized as follows:

  • Hydrophobic properties: Norcarane is primarily insoluble in water due to its non-polar nature, which inhibits interaction with polar water molecules.
  • Solvent compatibility: It demonstrates good solubility in organic solvents such as:
    • Hexane
    • Toluene
    • Ethanol
  • Saturation behavior: Norcarane's solubility can increase with temperature, indicating increased molecular motion that facilitates interactions with solvent molecules.

In summary, while norcarane shows limited solubility in polar solvents like water, it can effectively dissolve in non-polar organic solvents. This property underlines the importance of considering solvent polarity when using norcarane in chemical applications. As quoted from a notable research study, “the behavior of hydrocarbons in diverse environments is critical for applications ranging from industrial processes to environmental chemistry.”

Interesting facts

Interesting Facts About Norcarane

Norcarane is a fascinating cyclic hydrocarbon that captures the attention of researchers and students alike due to its unique structure and properties. Here are some intriguing facts about this compound:

  • Cyclic Structure: Norcarane features a bicyclic structure that is chemically distinct from other hydrocarbons. This unique configuration contributes to its interesting reactivity and potential applications.
  • Discovery: Norcarane was first synthesized in the 1980s. Since then, it has piqued the interest of many chemists for its intriguing chemical behavior.
  • Reactivity: Due to its strained ring system, norcarane is more reactive than many other alicyclic hydrocarbons. This characteristic makes it an interesting subject for studies focused on chemical reactivity and mechanistic pathways.
  • Potential Applications: Though it is primarily of academic interest, norcarane and its derivatives hold promise in various fields, including materials science and organic synthesis.
  • Comparison: Norcarane is often compared to other hydrocarbons like bicyclo[3.3.0]octane, which makes it a key subject in studies of structural isomerism and stereochemistry.

As researchers delve deeper into the properties and reactions of norcarane, they continue to uncover its potential uses and the implications it may hold in synthetic chemistry. The compound serves as a stunning example of the diversity found within the realm of organic chemistry.

Synonyms
Norcarane
Bicyclo[4.1.0]heptane
286-08-8
14214-86-9
Butanal, 2,3-dihydroxy-
NSC-143399
2,3-Dihydroxybutyraldehyde
DTXSID10870493
WPHGSKGZRAQSGP-UHFFFAOYSA-N
NSC143399
AKOS015840955
DB-067952
Q680932