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503:(ITX) is used in the printing industry. Pharmaceutical drugs that are derivatives of thioxanthone include
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InChI=1S/C13H8OS/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1-8H COPY
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Except where otherwise noted, data are given for materials in their
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476:. This synthesis can be seen as a special case of the
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Thioxanthenone; 9-Oxothioxanthene; Thioxanthen-9-one
491:to give a yellow colored liquid with intense green
461:Thioxanthone can be prepared by the reaction of
382:273 °C (523 °F; 546 K) (940 hPa)
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487:Thioxanthone dissolves in concentrated
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372:211 °C (412 °F; 484 K)
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282:Key: YRHRIQCWCFGUEQ-UHFFFAOYSA-N
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495:. A mixture of the thioxanthone
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428:(at 25 °C , 100 kPa).
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480:. The reduction product is
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303:c1ccc2c(c1)c(=O)c3ccccc3s2
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478:Friedel-Crafts acylation
412:Magnetic susceptibility
501:isopropylthioxanthone
448:heterocyclic compound
576:at Wikimedia Commons
554:, 14th Edition, 1610
37:Preferred IUPAC name
469:in the presence of
389:Solubility in water
354: g·mol
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474:aluminium chloride
432:Infobox references
362:Pale yellow solid
45:-Thioxanthen-9-one
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572:Media related to
450:that is a sulfur
440:Chemical compound
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402:in sulfuric acid
394:Nearly insoluble
235:CompTox Dashboard
101:Interactive image
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528:Thioxanthone
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499:of 2- and 4-
493:fluorescence
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482:thioxanthene
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444:Thioxanthone
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60:Identifiers
52:Other names
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551:Merck Index
497:derivatives
359:Appearance
312:Properties
159:100.007.046
121:ChEMBL83371
515:References
509:lucanthone
505:hycanthone
400:Solubility
347:Molar mass
223:EOK1SAC304
132:ChemSpider
88:3D model (
67:CAS Number
471:catalytic
180:207-749-4
172:EC Number
584:Category
467:phosgene
456:xanthone
414:(χ)
405:Soluble
77:492-22-8
190:PubChem
452:analog
352:212.27
296:SMILES
112:ChEMBL
31:Names
465:with
446:is a
271:InChI
203:10295
90:JSmol
507:and
214:UNII
141:9873
530:at
454:of
240:EPA
193:CID
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538:^
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328:13
340:S
337:O
334:8
331:H
325:C
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43:H
41:9
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