Chromane
Names
Preferred IUPAC name
3,4-Dihydro-2H -1-benzopyran
Other names
Chroman; Benzodihydropyran; Benzoxane
Identifiers
116150
ChEBI
ChemSpider
EC Number
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
Properties
C 9 H 10 O
Molar mass
134.178 g·mol−1
Hazards
GHS labelling :[ 1]
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).
Chemical compound
Chromane (benzodihydropyran ) is a heterocyclic chemical compound with the chemical formula C9 H10 O.[ 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
References
^ "Chromane" . pubchem.ncbi.nlm.nih.gov . Retrieved 22 February 2024 .
^ Rindfusz, R. E. (April 1919). "Syntheses of Chromanes and Coumaranes". Journal of the American Chemical Society . 41 (4): 665– 670. doi :10.1021/ja01461a015 .
External links