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Open Access Articles- Top Results for Pyran

Pyran

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Pyran
2H-pyran
4H-pyran

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IUPAC name
2H-Pyran, 4H-Pyran
Other names
2H-Oxine, 4H-Oxine
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289-66-7 (2H) 7pxN
289-65-6 (4H) 7pxN ChemSpider 161812 (2H) 7pxN
119912 (4H) 7pxN Jmol-3D images Image

(2H)
Image (4H)

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C5H6O Molar mass Lua error in Module:Math at line 495: attempt to index field 'ParserFunctions' (a nil value). g·mol−1 colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
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Related compounds
Dihydropyran
Tetrahydropyran
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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In chemistry, pyran, or oxine, is a six-membered heterocyclic, non-aromatic ring, consisting of five carbon atoms and one oxygen atom and containing two double bonds. The molecular formula is C5H6O. There are two isomers of pyran that differ by the location of the double bonds. In 2H-pyran, the saturated carbon is at position 2, whereas, in 4H-pyran, the saturated carbon is at position 4.

4H-Pyran was first isolated and characterized in 1962 via pyrolysis of 2-acetoxy-3,4-dihydro-2H-pyran.[1] It was found too unstable, particularly in the presence of air. 4H-pyran easily disproportionates to the corresponding dihydropyran and the pyrylium ion, which is easily hydrolyzed in aqueous medium.

Although the pyrans themselves have little significance in chemistry, many of their derivatives are important biological molecules, such as the pyranoflavonoids.

The term pyran is also often applied to the saturated ring analog, which is more properly referred to as tetrahydropyran (oxane). In this context, the monosaccharides containing a six-membered ring system are known as pyranoses.

See also

References

  1. ^ Masamune, S.; Castellucci, N. T. (1962). "γ-Pyran". Journal of the American Chemical Society 84 (12): 2452–2453. doi:10.1021/ja00871a037.