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Camphor oxime

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Identification
Molecular formula
C10H17NO
CAS number
4780-75-2
IUPAC name
1,7,7-trimethylnorbornan-2-one oxime
State
State

Camphor oxime is a solid under room temperature conditions. It can be handled as a typical crystalline substance, and it is relatively stable when stored properly.

Melting point (Celsius)
118.00
Melting point (Kelvin)
391.15
Boiling point (Celsius)
246.00
Boiling point (Kelvin)
519.15
General information
Molecular weight
167.25g/mol
Molar mass
167.2370g/mol
Density
1.0330g/cm3
Appearence

Camphor oxime appears as a white crystalline solid. It is typically odorless or has a light camphor-like smell. The crystals may have a specific texture and shine under the right lighting conditions.

Comment on solubility

Solubility of 1,7,7-Trimethylnorbornan-2-one Oxime

1,7,7-Trimethylnorbornan-2-one oxime typically exhibits interesting solubility properties based on its chemical structure. The solubility of this compound can be influenced by several factors:

  • Polarity: Due to the presence of the oxime functional group, the compound can engage in hydrogen bonding, potentially increasing its solubility in polar solvents.
  • Solvent Interaction: It is likely to be soluble in solvents such as alcohols or acetone, but may have limited solubility in non-polar solvents like hexane.
  • Temperature Effects: As with many organic compounds, solubility can increase with temperature, making it essential to consider the conditions under which the compound is dissolved.

To summarize, 1,7,7-trimethylnorbornan-2-one oxime is expected to be more soluble in polar environments due to its functional groups. Thus, it’s crucial for researchers and chemists to consider these factors when working with this compound to facilitate desired reactions or applications.

Interesting facts

Interesting Facts about 1,7,7-Trimethylnorbornan-2-one Oxime

1,7,7-trimethylnorbornan-2-one oxime is a fascinating organic compound with a variety of intriguing characteristics that make it an interesting subject of study. Here are some notable aspects:

  • Structural Intricacies: This compound belongs to the family of norbornanes, which feature a unique bridged bicyclic structure that makes them particularly stable and interesting from a stereochemical perspective.
  • Oxime Formation: The presence of the oxime functional group (–C=N–OH) is notable for its ability to participate in versatile chemical reactions. Oximes can be readily converted into other functional groups, making them valuable intermediates in organic synthesis.
  • Potential Applications: Due to its unique structure, 1,7,7-trimethylnorbornan-2-one oxime could find applications in fields such as medicinal chemistry and materials science. Compounds with similar structural motifs are often explored for their properties as pharmaceuticals or as precursors in polymer chemistry.
  • Isomeric Diversity: The ability to have different stereoisomers highlights the compound's complexity and potential for study. Scientists are often fascinated by how different configurations can yield compounds with varied physical and chemical properties.
  • Synthetic Routes: The synthesis of oxime compounds generally involves the reaction of aldehydes or ketones with hydroxylamine. This makes it a crucial compound in understanding synthetic organic chemistry techniques.

Overall, 1,7,7-trimethylnorbornan-2-one oxime serves as an excellent example of how structural complexity in organic compounds can lead to a wealth of research opportunities. As a chemist, one can appreciate the elegance of its structure and the potential for innovation in its applications.

Synonyms
Camphor oxime
D-Camphor oxime
N-[(2E)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ylidene]hydroxylamine
1,7,7-trimethylnorbornan-2-one oxime
Maybridge1_002074
SCHEMBL3081945
HMS2267K06
AKOS016874620
DB-047304
NS00085673
NS00085882
F0848-0342
(+/-)-1,7,7-trimethyl-bicyclo(2.2.1)heptane-2-one-oxime
(+/-)-1,7,7-trimethyl-bicyclo[2,2,1]heptane-2-one-oxime
(1S,4R,E)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one oxime
1,7,7-TRIMETHYL-BICYCLO(2.2.1)HEPTAN-2-ONE OXIME
(NE)-N-[(1R,4R)-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanylidene]hydroxylamine