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Camphene thiocyanate

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Identification
Molecular formula
C11H17NS
CAS number
146452-78-2
IUPAC name
(1,7,7-trimethylnorbornan-2-yl) thiocyanate
State
State
At room temperature, camphene thiocyanate can exist as a liquid with a pale yellow to reddish-brown appearance. However, it can crystallize into a solid due to its specific compound structure and the presence of the thiocyanate group.
Melting point (Celsius)
32.00
Melting point (Kelvin)
305.15
Boiling point (Celsius)
265.00
Boiling point (Kelvin)
538.15
General information
Molecular weight
207.33g/mol
Molar mass
207.3270g/mol
Density
1.0534g/cm3
Appearence

Camphene thiocyanate typically appears as a pale yellow to reddish-brown liquid. It may also crystallize into a solid under certain conditions. Due to the thiocyanate group, it can have a distinct odor.

Comment on solubility

Solubility of (1,7,7-trimethylnorbornan-2-yl) thiocyanate

The solubility of (1,7,7-trimethylnorbornan-2-yl) thiocyanate in various solvents exhibits intriguing characteristics due to its unique structure. This compound is a member of the thiocyanate family, which often displays interesting solubility profiles based on the polarity of the solvent used.

Solubility Characteristics:

  • Solvent Polarity: The solubility of this compound is expected to be higher in polar solvents due to the presence of the thiocyanate group, which is known to interact favorably with polar solvents.
  • Non-Polar Solvents: Conversely, solubility might be lower in non-polar solvents, as the bulky structure of the trimethyl groups can create steric hindrance, limiting interaction with such solvents.
  • Temperature Effects: Generally, increasing the temperature can enhance solubility, as it allows for increased molecular motion and interactions.

In practical applications, this solubility understanding is vital for the effective use of (1,7,7-trimethylnorbornan-2-yl) thiocyanate in various chemical processes and formulations. As a guideline, one might say that “a compound is usually most soluble in a solvent of similar polarity." Therefore, further experimentation may be required to determine its solubility in specific solvents, especially for optimal usage in chemical synthesis or formulation design.

Interesting facts

Interesting Facts about (1,7,7-trimethylnorbornan-2-yl) thiocyanate

(1,7,7-trimethylnorbornan-2-yl) thiocyanate is a fascinating compound that blends organic chemistry with structural complexity. Here are some key highlights about this intriguing molecule:

  • Unique Structure: The compound features a norbornane framework, characterized by its bicyclic system, which contributes to its interesting chemical behaviors and properties.
  • Thiocyanate Group: Incorporating a thiocyanate (–SCN) group provides the compound with potential applications in organic synthesis and coordination chemistry. Thiocyanates are known for their versatility.
  • Source of Study: Researchers often study thiocyanates for their biological activity. Compounds with the thiocyanate group can exhibit antimicrobial and cytotoxic properties, making them of interest in medicinal chemistry.
  • Applications: This compound can potentially serve in the creation of new materials or as a reagent in chemical reactions due to the presence of the reactive thiocyanate group.
  • Synthesis: The synthesis of this compound involves nuanced reactions and is a testament to the creativity required in organic synthesis, making it a valuable example for chemistry students.

In summary, (1,7,7-trimethylnorbornan-2-yl) thiocyanate is not just a chemical compound but a representation of how intricate molecular structures can lead to diverse applications in science. As one explores its properties and reactivity, it unveils a world of possibilities for innovation and research.

Synonyms
7492-22-0
Thiocyanic acid, 4,7,7-trimethylbicyclo(2.2.1)hept-2-yl ester, exo-
Thiocyanic acid, 4,7,7-trimethylbicyclo(2.2.1)hept-2-yl ester, exo-(9CI)
ISOBORNYL THIOCYANATE
SCHEMBL9691369
DTXSID90996403
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl thiocyanate