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Isobornyl methacrylate

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Identification
Molecular formula
C14H22O2
CAS number
7534-94-3
IUPAC name
(1,7,7-trimethylnorbornan-2-yl) 2-methylprop-2-enoate
State
State

At room temperature, isobornyl methacrylate is typically a liquid. It remains fluid and is not prone to solidifying under normal conditions, making it easy to handle and use in various applications.

Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
208.29g/mol
Molar mass
208.2860g/mol
Density
1.0061g/cm3
Appearence

Isobornyl methacrylate is often seen as a colorless liquid. It is known for its transparency and is usually clear, though it may have a slightly yellowish to light amber tint over time or upon exposure to air and light.

Comment on solubility

Solubility of (1,7,7-trimethylnorbornan-2-yl) 2-methylprop-2-enoate

(1,7,7-trimethylnorbornan-2-yl) 2-methylprop-2-enoate is a compound with intriguing solubility characteristics, which play a crucial role in its application and use. Understanding its solubility can help in various fields such as pharmaceuticals, materials science, and chemical synthesis.

Typically, the solubility of a compound depends on several factors including:

  • Polarity: This compound is expected to exhibit some degree of hydrophobicity due to its bulky hydrophobic substituents, which may limit its solubility in polar solvents.
  • Temperature: Solubility can increase with temperature. Therefore, the behavior of this compound may differ at varying temperature conditions.
  • Intermolecular forces: The presence of weak intermolecular forces such as van der Waals forces may affect how well this compound can solubilize in different solvents.
  • Possible interactions: Potential interactions with other molecules in a solution, such as hydrogen bonding or ion-dipole interactions, can also influence solubility.

In general, it can be said that:

  • It is likely soluble in non-polar solvents.
  • Its solubility in polar solvents is expected to be quite limited.

Thus, to use (1,7,7-trimethylnorbornan-2-yl) 2-methylprop-2-enoate effectively, one must consider these solubility traits. As the saying goes, "The right solvent can make all the difference!" This highlights the importance of choosing the correct solvent to optimize the use of this compound in various applications.

Interesting facts

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

(1,7,7-trimethylnorbornan-2-yl) 2-methylprop-2-enoate is a fascinating organic compound that showcases the intriguing intersection of structure and function in organic chemistry. Here are some highlights:

  • Synthetic Versatility: This compound is often used as a model in synthetic organic chemistry. Its unique structure makes it an excellent precursor for the synthesis of various biologically active molecules.
  • Reactivity: The presence of the 2-methylprop-2-enoate moiety introduces reactive double bonds, enabling diverse reactions such as nucleophilic additions and polymerization. This opens up exciting pathways for creating new materials.
  • Chiral Center: With multiple chirality centers present, this compound exemplifies the importance of stereochemistry in organic reactions. Understanding how stereoisomers behave differently can provide insights into reaction pathways and mechanisms.
  • Natural Analogues: Compounds similar to this one can be found in nature, often contributing to the aromas and flavors of various plants. Studying such compounds can reveal valuable information for applications in flavor chemistry and perfumery.
  • Applications in Materials Science: The unique properties of the compound may lend themselves well to the development of new polymeric materials, which is a burgeoning area of research aimed at creating sustainable and innovative materials.

In summary, (1,7,7-trimethylnorbornan-2-yl) 2-methylprop-2-enoate is more than just a compound; it's a gateway to understanding complex chemical interactions and pathways that are essential in both natural and synthetic chemistry. Exploring its properties and reactivity can spark creativity and innovation in multiple fields.

Synonyms
16868-12-5
2-Bornyl methacrylate
DTXSID10860016
DTXCID20209437
7534-94-3
ISOBORNYL 2-METHYL-2-PROPENOATE
Methacrylic acid isobornyl ester
(1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl) 2-methylprop-2-enoate
Isobornylmethacrylate
1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl methacrylate
IBMA
28854-39-9
bornyl methacrylate
Isobornyl Methacrylate (stabilized with MEHQ)
SCHEMBL33519
1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl 2-methylprop-2-enoate
AKOS015899918
NCGC00249187-01
I0617
NS00011468