Jump to content

Chromane

From Wikipedia, the free encyclopedia
(Redirected from Chromans)
Chromane
Names
Preferred IUPAC name
3,4-Dihydro-2H-1-benzopyran
Other names
Chroman; Benzodihydropyran; Benzoxane
Identifiers
3D model (JSmol)
116150
ChEBI
ChemSpider
EC Number
  • 874-955-4
122981
UNII
  • InChI=1S/C9H10O/c1-2-6-9-8(4-1)5-3-7-10-9/h1-2,4,6H,3,5,7H2
    Key: VZWXIQHBIQLMPN-UHFFFAOYSA-N
  • InChI=1/C9H10O/c1-2-6-9-8(4-1)5-3-7-10-9/h1-2,4,6H,3,5,7H2
    Key: VZWXIQHBIQLMPN-UHFFFAOYAB
  • C1CC2=CC=CC=C2OC1
Properties
C9H10O
Molar mass 134.178 g·mol−1
Hazards
GHS labelling:[1]
GHS02: FlammableGHS07: Exclamation mark
Warning
H226, H302, H315, H319, H335
P210, P233, P240, P241, P242, P243, P261, P264, P264 P265, P270, P271, P280, P301 P317, P302 P352, P303 P361 P353, P304 P340, P305 P351 P338, P319, P321, P330, P332 P317, P337 P317, P362 P364, P370 P378, P403 P233, P403 P235, P405, P501
Related compounds
Related compounds
Tetrahydroquinoline, Tetralin, Chromene, Coumaran
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Chromane (benzodihydropyran) is a heterocyclic chemical compound with the chemical formula C9H10O.[2] Chromane is a structural feature of more complex compounds including E vitamins (tocopherols and tocotrienols), Dianin's compound, and the pharmaceutical drugs troglitazone, ormeloxifene, and nebivolol. Such compounds are sometimes described as chromans.

See also

[edit]

References

[edit]
  1. ^ "Chromane". pubchem.ncbi.nlm.nih.gov. Retrieved 22 February 2024.
  2. ^ Rindfusz, R. E. (April 1919). "Syntheses of Chromanes and Coumaranes". Journal of the American Chemical Society. 41 (4): 665–670. doi:10.1021/ja01461a015.
[edit]