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they have disappeared over time from the market. However, since their light resistance is significantly better on
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rings. It occurs as the central core of a number of naturally occurring chemical compounds such as
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Nomenclature of
Organic Chemistry: IUPAC Recommendations and Preferred Names 2013
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Phenoxazine dyes were once widely used for silk dyeing, but due to their lack of
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Except where otherwise noted, data are given for materials in their
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InChI=1S/C12H9NO/c1-3-7-11-9(5-1)13-10-6-2-4-8-12(10)14-11/h1-8,13H
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InChI=1/C12H9NO/c1-3-7-11-9(5-1)13-10-6-2-4-8-12(10)14-11/h1-8,13H
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475:"Five- and six-membered rings with two or more heteroatoms"
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435:International Union of Pure and Applied Chemistry
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370:. The structure of phenoxazine consists of an
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394:are also based on a phenoxazine core.
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256:Key: TZMSYXZUNZXBOL-UHFFFAOYSA-N
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266:Key: TZMSYXZUNZXBOL-UHFFFAOYAS
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508:. You can help Knowledge (XXG) by
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348:(at 25 °C , 100 kPa).
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502:heterocyclic compound
500:This article about a
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368:heterocyclic compound
37:Preferred IUPAC name
338: g·mol
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352:Infobox references
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477:. britannica.com.
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52:Identifiers
45:-Phenoxazine
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17:Phenoxazine
386:. The dyes
364:Phenoxazine
296:Properties
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113:CHEBI:94057
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421:References
331:Molar mass
197:C2ZWT499SG
124:ChemSpider
80:3D model (
59:CAS Number
388:Nile blue
437:(2014).
409:See also
392:Nile red
69:135-67-1
376:benzene
372:oxazine
336:183.210
164:PubChem
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384:litmus
280:SMILES
31:Names
504:is a
366:is a
245:InChI
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133:60610
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455:ISBN
390:and
382:and
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321:N
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