Benzoxazole

Benzoxazole
Skeletal formula with numbering convention
Full structural formula with aromatic bond
Ball-and-stick molecular model
Space-filling molecular model
Names
Preferred IUPAC name
1,3-Benzoxazole
Other names
1-Oxa-3-aza-1H-indene
Identifiers
CAS Number
  • 273-53-0 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:38814 checkY
ChEMBL
  • ChEMBL451894 checkY
ChemSpider
  • 8873 checkY
ECHA InfoCard 100.005.445 Edit this at Wikidata
PubChem CID
  • 9228
UNII
  • J233Y1I55I checkY
CompTox Dashboard (EPA)
  • DTXSID8059768 Edit this at Wikidata
InChI
  • InChI=1S/C7H5NO/c1-2-4-7-6(3-1)8-5-9-7/h1-5H checkY
    Key: BCMCBBGGLRIHSE-UHFFFAOYSA-N checkY
  • InChI=1/C7H5NO/c1-2-4-7-6(3-1)8-5-9-7/h1-5H
    Key: BCMCBBGGLRIHSE-UHFFFAOYAP
  • n1c2ccccc2oc1
Properties
Chemical formula
 C7H5NO
Molar mass 119.123 g·mol−1
Appearance White to light yellow solid
Melting point 27 to 30 °C (81 to 86 °F; 300 to 303 K)
Boiling point 182 °C (360 °F; 455 K)
Solubility in water
 Insoluble
Hazards
Flash point 58 °C (136 °F; 331 K)
Related compounds
Related compounds
 oxazole
indole
benzofuran
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Chemical compound

Benzoxazole is an aromatic organic compound with a molecular formula C7H5NO, a benzene-fused oxazole ring structure, and an odor similar to pyridine.[1][2] Although benzoxazole itself is of little practical value, many derivatives of benzoxazoles are commercially important.

Being a heterocyclic compound, benzoxazole finds use in research as a starting material for the synthesis of larger, usually bioactive structures. Its aromaticity makes it relatively stable, although as a heterocycle, it has reactive sites which allow for functionalization.

Occurrence and applications

It is found within the chemical structures of pharmaceutical drugs such as flunoxaprofen and tafamidis. Benzoxazole derivatives are also of interest for optical brighteners in laundry detergents.[3] Benzoxazoles belong to the group of well-known antifungal agents with antioxidant, antiallergic, antitumoral and antiparasitic activity.[4]

  • 4,4'-(E)-bis(benzoxazolyl)stilbene is intensely fluorescent and its derivatives are used as optical brighteners
    4,4'-(E)-bis(benzoxazolyl)stilbene is intensely fluorescent and its derivatives are used as optical brighteners
  • 2,5-bis(benzoxazol-2-yl)thiophene is also intensely fluorescent and its derivatives are used as optical brighteners, e.g. in laundry detergents[5]
    2,5-bis(benzoxazol-2-yl)thiophene is also intensely fluorescent and its derivatives are used as optical brighteners, e.g. in laundry detergents[5]

See also

Structural isomers
Analogs

References

  1. ^ Katritzky, A. R.; Pozharskii, A. F. (2000). Handbook of Heterocyclic Chemistry (2nd ed.). Academic Press. ISBN 0080429882.
  2. ^ Clayden, J.; Greeves, N.; Warren, S.; Wothers, P. (2001). Organic Chemistry. Oxford, Oxfordshire: Oxford University Press. ISBN 0-19-850346-6.
  3. ^ E. Smulders, E. Sung "Laundry Detergents, 2. Ingredients and Products" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2012. doi:10.1002/14356007.o15_013
  4. ^ Şener, E., Yalçin, İ. and Sungur, E.: QSAR of some antifungal benzoxazoles and oxazolo(4,5-b)pyridines against C. Albicans. Quant. Struct.-Act. Relat. 10 (1991) 223-228.
  5. ^ Fourati, M. Amine; Maris, Thierry; Skene, W. G.; Bazuin, C. Géraldine; Prud’homme, Robert E. (3 November 2011). "Photophysical, Electrochemical and Crystallographic Investigations of the Fluorophore 2,5-Bis(5-tert-butyl-benzoxazol-2-yl)thiophene". The Journal of Physical Chemistry B. 115 (43): 12362–12369. doi:10.1021/jp207136k. PMID 21916450.