Xanthene
From Wikipedia, the free encyclopedia
Not to be confused with xanthine.
| Xanthene | |
|---|---|
 |
|
| IUPAC name | 9H-Xanthene |
| Other names | Dibenzo[a,e]pyran 10H-9-oxaanthracene |
| Identifiers | |
| CAS number | [] |
| EINECS number | |
| SMILES | c1(Oc2ccccc2C3)c3cccc1 |
| Properties | |
| Molecular formula | C13H10O |
| Molar mass | 182.22 g/mol |
| Appearance | Yellow solid |
| Melting point |
101-102 °C |
| Boiling point |
310-312 °C |
| Hazards | |
| R-phrases | R42 R43 |
| S-phrases | S22 S36 S37 S45 |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
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Xanthene (9H-xanthene, 10H-9-oxaanthracene) is a yellow organic heterocyclic compound. Its chemical formula is C13H10O. It is soluble in ether. Its melting point is 101-102 °C and its boiling point is 310-312 °C.
Xanthene is used in organic synthesis. It is used as a fungicide.
Xanthene is a basis of a class of dyes; eg. fluorescein, eosins, and rhodamines are derived from its structure. Xanthene dyes tend to be fluorescent, yellow to pink to bluish red, brilliant dyes.
Many xanthene dyes can be prepared by condensation of derivates of phthalic anhydride with derivates of resorcinol or 3-aminophenol.
Xanthene can also be used as a name of any of xanthene derivates.
