| Identification | Back Directory | [Name]
THIOQUINOX | [CAS]
93-75-4 | [Synonyms]
readex
ss1451
B-31686
bay30686
ent25,579
Ai3-25579
THIOQUINOX
ss1451[qr]
thiaquinox
bayer30686
Brn 0521713
CHINOTHIONAT
bay30686[qr]
eraditon[qr]
erazidon[qr]
ent25,579[qr]
bayer4935[qr]
QUINOTHIONATE
Chinothionate
bayer31686[qr]
thioquinox (bsi,iso)
chinoxalin-2,3-diyl-trithiocarbonat
2-thio-1,3-dithio(4,5-b)quinoxaline
quinoxaline-2,3-diyltrithiocarbonate
2-thio-1,3-dithiolo[4,5-b]quinoxaline
chinoxalin-2,3-diyl-trithiocarbonat[qr]
1,3-dithiolo(4,5-b)quinoxaline-2-thione
2-THIOXO-1,3-DITHIOLO(4,5-B)QUINOXALINE
2-thio-1,3-dithiolo[4,5-b]quinoxaline[qr]
chinoxalin-2,3-dithiol-cyclo-thio-carbonat
2,3-quinoxalinedithiol,cyclictrithiocarbonate
thioquinox 2-thio-1,3-dithiolo(4,5,b)quinoxaline
2-thio-1,3-dithiolo(4,5,b)quinoxaline,thioquinox
carbonicacid,trithio-,cyclic2,3-quinoxalinediylester
trithiocarbonicacidcyclic2,3-quinoxalinediylester[qr]
trithiocarbonicacid,cyclicesterwith2,3-quinoxalinedithiol
carbonicacid,trithio-,cyclicesterwith2,3-quinoxalinedithiol | [EINECS(EC#)]
202-272-8 | [Molecular Formula]
C9H4N2S3 | [MDL Number]
MFCD00145403 | [MOL File]
93-75-4.mol | [Molecular Weight]
236.34 |
| Hazard Information | Back Directory | [Chemical Properties]
Yellow solid. Insoluble in
water; slightly soluble in acetone, kerosene, and
alcohol. | [Uses]
Acaricide, fungicide. | [Definition]
ChEBI: Thioquinox is a quinoxaline acaricide, a quinoxaline antifungal agent and a dithioloquinoxaline. | [Production Methods]
The production route for thioquinox is not available in open literature. However, it can be inferred from its structure. Commercial production would probably have followed the standard logic for quinoxaline based heterocycles: construction of the quinoxaline core, introduction of dithiol units, and final cyclisation to form the trithiocarbonate ring system. After ring closure, the crude product would be purified by crystallisation, filtration, and drying to yield technical grade thioquinox for formulation. | [Hazard]
Toxic by ingestion. | [Mechanism of action]
Binds with amino and mercapto groups resulting in the inhibition of various enzymes | [Pesticide Type]
Insecticide; Acaricide; Ovicide; Fungicide |
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