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Camphor 2-thiocyanatoacetate

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Identification
Molecular formula
C13H17NO2S
CAS number
3616-43-5
IUPAC name
(1,7,7-trimethylnorbornan-2-yl) 2-thiocyanatoacetate
State
State

At room temperature, (1,7,7-Trimethylnorbornan-2-yl) 2-thiocyanatoacetate is typically found in a solid state.

Melting point (Celsius)
102.50
Melting point (Kelvin)
375.70
Boiling point (Celsius)
270.50
Boiling point (Kelvin)
543.70
General information
Molecular weight
239.32g/mol
Molar mass
239.3230g/mol
Density
1.2000g/cm3
Appearence

(1,7,7-Trimethylnorbornan-2-yl) 2-thiocyanatoacetate is typically a crystalline solid with a white to off-white color. The crystals may have a glossy appearance due to their well-defined structure. The compound is often used in a variety of industrial applications due to its stability and reactivity.

Comment on solubility

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

(1,7,7-trimethylnorbornan-2-yl) 2-thiocyanatoacetate exhibits intriguing solubility characteristics, primarily influenced by its unique structure. When considering its solubility in various solvents, a few key points emerge:

  • Polar solvents: The presence of the thiocyanato group can enhance solubility in polar solvents such as water and alcohols due to potential hydrogen bonding and dipole interactions.
  • Non-polar solvents: Conversely, the bulky norbornane structure typically favors solubility in non-polar solvents like hexane and toluene.
  • Intermediate behavior: In mixed solvents, (1,7,7-trimethylnorbornan-2-yl) 2-thiocyanatoacetate may demonstrate intermediate solubility, showcasing versatility depending on the solvent composition.

The balance between its polar and non-polar characteristics makes it an interesting compound for studies in solubility dynamics. As with many organic compounds, temperature may also play a role, with increased temperature generally enhancing solubility in both polar and non-polar solvents:

  1. As temperature rises, the kinetic energy of molecules increases, potentially leading to better dissolution.
  2. Chemical interactions, such as hydrogen bonding in polar environments, may also be favored.

In summary, the solubility profile of (1,7,7-trimethylnorbornan-2-yl) 2-thiocyanatoacetate reflects its complex structural attributes and offers a fascinating area for further exploration within the realm of chemical compounds.

Interesting facts

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

(1,7,7-trimethylnorbornan-2-yl) 2-thiocyanatoacetate is a fascinating compound that showcases the intricate dance between organic chemistry and synthesis. Here are some intriguing aspects of this compound:

  • Structural Diversity: The compound features a norbornane structure, which is known for its unique cage-like arrangement. This structural diversity contributes to its interesting chemical properties.
  • Functional Groups: The presence of a thiocyanate group introduces *polar functionality* to the compound, making it a point of interest for studying reactivity and solubility.
  • Applications: Compounds like this one can play a pivotal role in medicinal chemistry, especially in the design of drugs. The thiocyanate group has shown promise in enhancing biological activity.
  • Synthesis Potential: This compound serves as a building block in organic synthesis, opening doors to further functionalization and modification within complex synthetic pathways.
  • Research Interest: Due to its unique characteristics, it attracts attention in various fields including catalysis, materials science, and chemical biology.

As you delve into the study of (1,7,7-trimethylnorbornan-2-yl) 2-thiocyanatoacetate, you will uncover the *rich tapestry* of interactions that inherently define the behavior of organic compounds. Investigating its properties not only advances our understanding of chemical principles but also contributes to innovations in material and pharmaceutical science.

Synonyms
ISOBORNYL THIOCYANOACETATE
Isobornyl thiocyanatoacetate
20285-28-3
(1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl) 2-thiocyanatoacetate
5339-57-1
SCHEMBL790530
1,7,7-Trimethylbicyclo[2.2.1]hept-2-yl (cyanosulfanyl)acetate #
Acetic acid, thiocyanato-, 1,7,7-trimethylbicyclo(2.2.1)hept-2-yl ester
DTXSID10859208
IXEVGHXRXDBAOB-UHFFFAOYSA-N
1,7,7-trimethylbicyclo[2.2.1]hept-2-yl (cyanothio)acetate
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl (thiocyanato)acetate