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Oxazole

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Identification
Molecular formula
C3H3NO
CAS number
288-42-6
IUPAC name
oxazole
State
State

At room temperature, oxazole is a liquid.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.00
Boiling point (Celsius)
69.00
Boiling point (Kelvin)
342.00
General information
Molecular weight
69.07g/mol
Molar mass
69.0710g/mol
Density
1.0510g/cm3
Appearence

Oxazole is a pale yellow liquid.

Comment on solubility

Solubility of Oxazole

Oxazole, a heterocyclic compound characterized by a five-membered ring containing both nitrogen and oxygen, displays unique solubility properties that are influenced by its molecular structure. The solubility of oxazole in various solvents can be summarized as follows:

  • Polar solvents: Oxazole is generally soluble in polar solvents such as water and alcohols due to the presence of the electronegative nitrogen and oxygen atoms, which engage in hydrogen bonding.
  • Non-polar solvents: It has limited solubility in non-polar solvents due to its polar functional groups, making it less favorable for dissolution in these environments.
  • Protic solvents: Oxazole shows enhanced solubility in protic solvents, where the ability of the solvent to form hydrogen bonds further facilitates the solubility of oxazole.
  • Temperature dependency: The solubility of oxazole can also be affected by temperature; typically, increased temperatures enhance the solubility of solid oxazole in liquid solvents.

In summary, the solubility of oxazole is influenced by:

  1. The nature of the solvent (polar vs. non-polar)
  2. The temperature at which dissolution occurs
  3. The molecular interactions between oxazole and the solvent

As scientists and chemists, understanding these solubility characteristics is crucial for practical applications, including synthesis and formulation in various chemical processes.

Interesting facts

Interesting Facts about Oxazole

Oxazole is a fascinating heterocyclic compound that belongs to the class of aromatic compounds. This five-membered ring contains both nitrogen and oxygen atoms, which contribute to its unique chemical properties and reactivity. Here are some key points that make oxazole particularly interesting:

  • Structure: The structure of oxazole features a five-membered ring containing one nitrogen and one oxygen atom. This configuration leads to a wealth of derivatives with various functional properties.
  • Reactivity: Oxazole can act as a weak Lewis base due to the lone pair of electrons on the nitrogen atom, making it capable of engaging in multiple chemical reactions.
  • Biological Significance: Oxazole derivatives are often found in nature and play a crucial role in biological systems. For instance, some compounds containing the oxazole structure exhibit antibacterial and antifungal activity, making them of interest in pharmaceutical research.
  • Synthesis: Several methods exist for synthesizing oxazole and its derivatives. For example, one common pathway involves the condensation of an amino acid with a carbonyl compound and an electrophile.
  • Applications: Beyond pharmaceuticals, oxazoles are useful in materials science and agriculture. They serve as precursors for the synthesis of various agrochemicals, enhancing crop protection.

As a student of chemistry, you might find it intriguing to explore the diverse applications of oxazole in the field of medicinal chemistry. The ability to modify its structure to design new compounds is a testament to the compound's versatility. In the words of one chemist, "Understanding the chemistry of heterocycles like oxazole opens up new avenues for innovation in drug design."
With its unique properties and applications, oxazole continues to be a subject of study and a source of inspiration for scientists worldwide.

Synonyms
OXAZOLE
1,3-Oxazole
288-42-6
3-Azafuran
Oxazoles
FJZ20I1LPS
CHEBI:35597
EINECS 206-020-8
MFCD00009751
DTXSID70182983
oxazol
Oxazole, 98%
UNII-FJZ20I1LPS
4-Methyl-5-EthoxyoxazoleOxazol
CHEMBL2171710
CHEBI:35790
DTXCID10105474
BBL103334
STL557144
AKOS005206966
FO26619
PB17048
HY-34631
DB-011626
CS-0020144
NS00014384
O0287
EN300-67789
AA-511/25015522
Q413437
F0001-0902
206-020-8