Skip to main content

Alkynylbenzoxazolone

ADVERTISEMENT
Identification
Molecular formula
C10H7NO2
CAS number
402931-91-3
IUPAC name
3-prop-2-ynyl-1,3-benzoxazol-2-one
State
State

At room temperature, Alkynylbenzoxazolone is typically found in a solid state.

Melting point (Celsius)
105.00
Melting point (Kelvin)
378.15
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
173.18g/mol
Molar mass
173.1810g/mol
Density
1.2000g/cm3
Appearence

Alkynylbenzoxazolone is generally a white to off-white crystalline solid. It can also appear as a powder.

Comment on solubility

Solubility of 3-prop-2-ynyl-1,3-benzoxazol-2-one

The solubility of 3-prop-2-ynyl-1,3-benzoxazol-2-one can be characterized by several factors that contribute to its behavior in various solvents. Here are some key considerations:

  • Polarity: The compound has a significant polar character due to the presence of the benzoxazole functional group, which can enhance its solubility in polar solvents.
  • Solvent Type: It may exhibit good solubility in common polar solvents such as methanol or ethanol while showing limited solubility in non-polar solvents like hexane.
  • pH Sensitivity: The solubility can also be influenced by the pH of the solution, as ionization of functional groups may occur in certain pH ranges, altering solubility characteristics.
  • Temperature Influence: Generally, increasing temperature may improve the solubility of organic compounds, and this may be true for 3-prop-2-ynyl-1,3-benzoxazol-2-one as well.

In summary, while specific solubility data for this compound may be limited, understanding the influence of structural attributes and environmental conditions is crucial for predicting its behavior in various solutions. Experimentation in different solvents can provide more concrete insights into its solubility profile.

Interesting facts

Interesting Facts about 3-prop-2-ynyl-1,3-benzoxazol-2-one

3-prop-2-ynyl-1,3-benzoxazol-2-one is a fascinating compound with significant implications in various fields of research. Known for its unique structure, it combines a benzoxazole moiety with an alkyne substituent, offering intriguing chemical properties. Here are some key points to consider:

  • Pharmacological Potential: Compounds containing the benzoxazole ring are often investigated for their biological activities. This compound has been noted for its potential antimicrobial and anticancer properties.
  • Fluorescent Properties: The structural configuration of 3-prop-2-ynyl-1,3-benzoxazol-2-one may contribute to its ability to exhibit fluorescence, making it valuable in biochemical imaging and sensor applications.
  • Conjugated System: The presence of the alkyne group in the compound allows for interesting conjugation effects, which can enhance its electronic properties and make it suitable for use in organic electronics.
  • Synthetic Versatility: Its unique structure poses interesting challenges and opportunities for synthetic chemists. Researchers are continually finding novel methods to synthesize and modify benzoxazole derivatives to increase their efficacy and applicability.

Furthermore, the study of such compounds not only expands our understanding of organic chemistry but also opens doors to potential innovations in drug development and materials science. As stated by chemists, "the discovery of nature's secrets through chemistry is a pursuit without end." Exploring 3-prop-2-ynyl-1,3-benzoxazol-2-one is a perfect example of how chemical compounds can lead to groundbreaking advancements.

In conclusion, 3-prop-2-ynyl-1,3-benzoxazol-2-one stands as an exciting compound for both its theoretical implications and practical applications within the fields of medicinal chemistry and material science. Its unique chemical architecture illustrates the beauty and complexity inherent in the world of chemistry.

Synonyms
19420-41-8
2-BENZOXAZOLINONE, 3-(2-PROPYNYL)-
BRN 1212483
3-(2-Propynyl)-2-benzoxazolinone
DTXSID00173041
DTXCID6095532
RefChem:256413
3-prop-2-ynyl-1,3-benzoxazol-2-one
3-(2-Propynyl)benzoxazol-2(3H)-one
3-(prop-2-yn-1-yl)benzo[d]oxazol-2(3H)-one
SCHEMBL3027838
AKOS008950831
3-(2-Propyn-1-yl)-2(3h)-benzoxazolone
DB-203649
3-(2-propynyl)-1,3-benzoxazol-2(3H)-one