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Home/Compounds/Research Reagent/2-chlorothioxanthone
C13H7ClOS
246.71 g/mol
Research ReagentDanger

2-Chlorothioxanthone

CAS86-39-5EC201-667-2
Category
Research Reagent
Compound Class
Heterocycle
Primary Use
Research Compound

2-Chlorothioxanthone is a research compound primarily utilized in phosphorescence studies. It has been investigated for its ability to induce highly efficient pure organic room-temperature phosphorescence through one-dimensional π–π stacking interactions.

research compound for phosphorescence studiesmaterials for organic phosphorescence research

Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.

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Referencesame scaffold

2-Trifluoromethyl thioxanthone

CAS1693-28-3

photoinitiator for polymerization reactions

Referencesame scaffold

2-isopropylthioxanthone

CAS5495-84-1

photoinitiator in printing

Referencesame scaffold

2,4-Diethyl-9H-thioxanthen-9-one

CAS82799-44-8

Photoinitiator for radical polymerization

Safety Reference

Flammable
Flammable
Danger
H228Flammable solid
Identifiers
IUPAC Name

2-chlorothioxanthen-9-one

InChIKey

ZCDADJXRUCOCJE-UHFFFAOYSA-N

SMILES

C1=CC=C2C(=C1)C(=O)C3=C(S2)C=CC(=C3)Cl

Synonyms (19)
  • Chlorprothixene EP Impurity E; Zuclopenthixol Decanoate EP Impurity B
  • Chlorprothixene Hydrochloride Imp. E (EP); Chlorprothixene Imp. E (EP); 2-Chloro-9H-thioxanthen-9-one; Chlorprothixene Hydrochloride Impurity E; Zuclopenthixol Decanoate Impurity B; Chlorprothixene Impurity E
  • Zuclopenthixol Decanoate EP Impurity B
  • Zuclopenthixol impurity B, European Pharmacopoeia (EP)
  • 2-Chloro-9H-thioxanthen-9-one
  • 2-Chlorothiaxanthone
  • 2-Chlorothioxanthen-9-one
  • 2-Chlorothioxanthone
  • 2-chloranylthioxanthen-9-one
  • 2-chloro-9-thioxanthenone
  • 2-chloro-9-thioxanthone
  • 2-chlorothioxanthene-9-one
  • 2-chlorothioxanthon
  • Thioxanthen-9-one, 2-chloro-
  • Zuclopenthixol impurity B CRS