Phenoxazine
 | |
| Names | |
|---|---|
| IUPAC name
10H-Phenoxazine | |
| Identifiers | |
| 135-67-1 | |
| 3D model (Jmol) | Interactive image |
| ChemSpider | 60610 |
| ECHA InfoCard | 100.004.737 |
| PubChem | 67278 |
| |
| |
| Properties | |
| C12H9NO | |
| Molar mass | 183.21 g·mol−1 |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Phenoxazine is a heterocyclic compound. The structure of phenoxazine consists of an oxazine fused to two benzene rings. It occurs as the central core of a number of naturally occurring chemical compounds such as dactinomycin and litmus. The dyes Nile blue and Nile red are also based on a phenoxazine core.
Phenoxazine dyes were once widely used for silk dyeing, but due to their lack of lightfastness they have disappeared over time from the market. However, since their light resistance is significantly better on acrylic fibers, these dyes have experienced a renaissance.
Phenoxazine has found application in the synthesis of Ragaglitazar.
See also
References
This article is issued from Wikipedia - version of the 8/18/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.