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Norborneol

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Identification
Molecular formula
C8H14O
CAS number
497-36-9
IUPAC name
norbornan-2-ylmethanol
State
State

At room temperature, norborneol is a solid. It is stable under normal temperatures and pressures.

Melting point (Celsius)
92.00
Melting point (Kelvin)
365.15
Boiling point (Celsius)
187.00
Boiling point (Kelvin)
460.15
General information
Molecular weight
126.20g/mol
Molar mass
126.1960g/mol
Density
1.0083g/cm3
Appearence

Norborneol appears as a white crystalline solid. It has a camphor-like odor, subtle, yet distinct due to the presence of the bicyclic structure.

Comment on solubility

Solubility of Norbornan-2-ylmethanol

Norbornan-2-ylmethanol, a bicyclic organic compound, presents intriguing properties concerning its solubility. When examining its behavior in various solvents, a few key points emerge:

  • Polar vs. Non-Polar Solvents: Due to the presence of a hydroxyl group (-OH), norbornan-2-ylmethanol tends to be soluble in polar solvents such as water and alcohols. This is attributable to hydrogen bonding interactions.
  • Hydrophobic Character: The bulky bicyclic structure can result in reduced solubility in highly polar solvents. It is often less soluble in non-polar solvents like hexane, highlighting the compound's complex solubility profile.
  • Temperature Influence: As with many organic compounds, an increase in temperature can enhance solubility, allowing for better dispersion in solvents.

In summary, the solubility of norbornan-2-ylmethanol showcases the balance between its polar functional groups and its bicyclic nature, making it an interesting compound for further exploration in various contexts.

Interesting facts

Interesting Facts about Norbornan-2-ylmethanol

The compound known as Norbornan-2-ylmethanol has garnered attention in the field of organic chemistry due to its unique structural characteristics and diverse applications. Here are some key points that highlight its significance:

  • Structural Uniqueness: Norbornan-2-ylmethanol is derived from norbornane, a bicyclic compound. This distinct structure provides it with interesting stereochemical properties, which can influence its reactivity and interactions with other molecules.
  • Precursor in Synthesis: This compound serves as an important precursor in the synthesis of various complex organic compounds. Its functional groups can be easily modified, making it a valuable building block in organic synthesis.
  • Potential Applications: Due to its alcohol functional group, Norbornan-2-ylmethanol may find applications in the pharmaceutical industry as an intermediate in the synthesis of bioactive compounds. Furthermore, its unique structure may lead to discovery of novel compounds with potential biological activities.
  • Impact on Chemical Research: Chemists are often intrigued by compounds like Norbornan-2-ylmethanol because they allow for the exploration of reaction mechanisms and chemical transformations, leading to a deeper understanding of organic reactions.
  • Chirality Considerations: The stereocenters present in Norbornan-2-ylmethanol can introduce chirality, often leading to the study of enantiomers and their distinct properties. This aspect is crucial in the design of chiral drugs which target specific biological pathways.

In summary, Norbornan-2-ylmethanol exemplifies the complexity and beauty of organic compounds. As researchers continue to study its properties and applications, it may pave the way for new discoveries in organic synthesis and pharmaceutical chemistry.

Synonyms
5240-72-2
Bicyclo[2.2.1]heptane-2-methanol
2-Norbornylmethanol
2-Norcamphanemethanol
2-(Hydroxymethyl)norbornane
2-Norcamphanylmethanol
2-Norkamfanylmethanol
2-Norcamphane methanol
CPC 1207
Experimental chemotherapeutant 1,207
2-Hydroxymethylnorcamphane
CC 1207
EC-1207
NSC 53599
NSC 55693
2-Norkamfanylmethanol [Czech]
Bicyclo(2.2.1)heptane-2-methanol
EINECS 226-041-6
2-Hydroxymethylbicyclo(2.2.1)heptane
BRN 2203428
AI3-08982
2-06-00-00062 (Beilstein Handbook Reference)
2-Hydroxymethylbicyclo[2.2.1]heptane
Bicyclo2.2.1heptane-2-methanol
226-041-6
2-NORBORNANEMETHANOL
Bicyclo[2.2.1]heptan-2-ylmethanol
Norbornane-2-methanol
2-norbornane methanol
2-bicyclo[2.2.1]heptanylmethanol
2-Hydroxymethylnorbornane
2-(Hydroxymethyl)norcamphane
2-(Hydroxymethyl)bicyclo[2.2.1]heptane
WLN: L55 ATJ C1Q
{bicyclo[2.2.1]heptan-2-yl}methanol
Methanol, 2-norbornane-
SCHEMBL75491
DTXSID70875762
NSC53599
NSC55693
Bicyclo(2,2,1)heptane-2-carbinol
bicyclo[2.2.1]hept-2-yl-methanol
Bicyclo[2.2.1]heptane-2-carbinol
Bicyclo[2.2.1]hheptane-2-methanol
NSC-53599
NSC-55693
(Bicyclo[2.2.1]hept-2-yl)methanol
AKOS009075809
Bicyclo[2.2.1]hept-2-ylmethanol #
LS-13473
SY053617
DB-003095
N0553
NS00045323
EN300-22337
2-NorbornanemethanolMixture of inner and outer shapes
Z147642452