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Details

Stereochemistry ACHIRAL
Molecular Formula C12H8OS
Molecular Weight 200.256
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENOXATHIIN

SMILES

O1C2=CC=CC=C2SC3=C1C=CC=C3

InChI

InChIKey=GJSGGHOYGKMUPT-UHFFFAOYSA-N
InChI=1S/C12H8OS/c1-3-7-11-9(5-1)13-10-6-2-4-8-12(10)14-11/h1-8H

HIDE SMILES / InChI

Molecular Formula C12H8OS
Molecular Weight 200.256
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Chemical fate and mutagenic formation potentials of phenothiazine and related compounds during water chlorination.
2010-12
Bovine and human serum albumin interactions with 3-carboxyphenoxathiin studied by fluorescence and circular dichroism spectroscopy.
2010-06-01
Is the anti-psychotic, 10-(3-(dimethylamino)propyl)phenothiazine (promazine), a potential drug with which to treat SARS infections? Lack of efficacy of promazine on SARS-CoV replication in a mouse model.
2008-08
Addition of the phenoxathiin cation radical to alkenes and nonconjugated dienes. Formation of (E)- and (Z)-(10-phenoxathiiniumyl)alkenes and (E)- and (Z)-(10-phenoxathiiniumyl)dienes on basic alumina.
2007-08-03
2-phenoxathiinyl-5-phenyloxazole and 5-phenoxathiinyl-2-phenyloxazole derivatives: experimental and theoretical study of emission properties.
2007-04
Aqueous solubility data for pressurized hot water extraction for solid heterocyclic analogs of anthracene, phenanthrene and fluorene.
2007-01-26
Reaction of thianthrene and phenoxathiin cation radicals with 2,3-dimethyl-2-butene. Chemical and electrochemical studies.
2006-05-12
Adducts of thianthrene- and phenoxathiin cation radical tetrafluoroborates to 1-alkynes. Structures and formation of 1-(5-thianthreniumyl)- and 1-(10-phenoxathiiniumyl)alkynes on alumina leading to alpha-ketoylides and alpha-ketols.
2005-11-25
Adducts of thianthrene- and phenoxathiin cation radical salts with symmetrical alkynes. Structure and formation of cumulenes on alumina leading to alpha-diketones, alpha-hydroxyalkynes, and alpha-acetamidoalkynes.
2005-05-13
Tuning emissive states in electrogenerated chemiluminescence.
2004-08-18
Adducts of phenoxathiin and thianthrene cation radicals with alkenes and cycloalkenes.
2003-11-14
Isolation and characterization of the genes encoding a novel oxygenase component of angular dioxygenase from the gram-positive dibenzofuran-degrader Terrabacter sp. strain DBF63.
2001-04-27
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:42:30 GMT 2025
Edited
by admin
on Mon Mar 31 18:42:30 GMT 2025
Record UNII
BJC51V8XW8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-464
Preferred Name English
PHENOXATHIIN
Systematic Name English
DIBENZOOXATHIANE
Systematic Name English
PHENOXTHIN
Common Name English
DIBENZOTHIOXIN
Systematic Name English
PHENOXATHIANE
Common Name English
PHENOTHIOXIN
Common Name English
1,4-DIBENZOTHIOXINE
Common Name English
PHENOXATHRIN
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 64301
Created by admin on Mon Mar 31 18:42:30 GMT 2025 , Edited by admin on Mon Mar 31 18:42:30 GMT 2025
Code System Code Type Description
PUBCHEM
9217
Created by admin on Mon Mar 31 18:42:30 GMT 2025 , Edited by admin on Mon Mar 31 18:42:30 GMT 2025
PRIMARY
WIKIPEDIA
Phenoxathiin
Created by admin on Mon Mar 31 18:42:30 GMT 2025 , Edited by admin on Mon Mar 31 18:42:30 GMT 2025
PRIMARY
EPA CompTox
DTXSID4024937
Created by admin on Mon Mar 31 18:42:30 GMT 2025 , Edited by admin on Mon Mar 31 18:42:30 GMT 2025
PRIMARY
FDA UNII
BJC51V8XW8
Created by admin on Mon Mar 31 18:42:30 GMT 2025 , Edited by admin on Mon Mar 31 18:42:30 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-975-8
Created by admin on Mon Mar 31 18:42:30 GMT 2025 , Edited by admin on Mon Mar 31 18:42:30 GMT 2025
PRIMARY
CAS
262-20-4
Created by admin on Mon Mar 31 18:42:30 GMT 2025 , Edited by admin on Mon Mar 31 18:42:30 GMT 2025
PRIMARY
NSC
464
Created by admin on Mon Mar 31 18:42:30 GMT 2025 , Edited by admin on Mon Mar 31 18:42:30 GMT 2025
PRIMARY