ChemicalBook--->CAS DataBase List--->2674-91-1

2674-91-1

2674-91-1 Structure

2674-91-1 Structure
IdentificationBack Directory
[Name]

ESP
[CAS]

2674-91-1
[Synonyms]

ESP
s410
estox
bay23655
thiometan
ent25,674
Ai3-25674
bayer23655
oxydeprofos
oxyphionfos
Brn 1711537
Oxideprofos
ESP STANDARD
metasystox-s
Caswell no. 366
Einecs 220-221-8
Epa pesticide chemical code 366100
s-2-etil-sulfinil-1-metil-etil-o,o-dimetil-monotiofosfato
S-2-ETHYLSULFINYL-1-METHYLETHYLO,O-DIMETHYLPHOSPHOROTHIOATE
o,o-dimethyl-s-(ethylsulfinyl-(2-isopropyl))phosphorothioate
s-2-aethylsulfinyl-1-methylaethyl-o,odimethyl-monothiophosphat
s-2-ethyl-sulfinyl-1-methyl-ethyl-o,o-dimethyl-monothiofosfaat
thiophosphatedeo,o-dimethyleetdes-2-(isopropylsulfinyl)-ethyle
s-(2-ethylsulphinyl-1-methylethyl)-o,o-dimethylphosphorothioate
o,o-dimethyls-(2-(ethylsulfinyl)-1-methylethyl)phosphorothioate
s-2-ethyl-sulphinyl-1-methyl-ethyl-o,o-dimethylphosphorothiolate
phosphorothioicacid,o,o-dimethyls-(ethylsulfinyl-(2-isopropyl))ester
Thiophosphoric acid O,O-dimethyl S-[2-(ethylsulfinyl)-1-methylethyl]
phosphorothioicacid,s-(2-(ethylsulfinyl)-1-methylethyl)o,o-dimethylester
[EINECS(EC#)]

220-221-8
[Molecular Formula]

C7H17O4PS2
[MDL Number]

MFCD01748336
[MOL File]

2674-91-1.mol
[Molecular Weight]

260.31
Chemical PropertiesBack Directory
[Boiling point ]

90.3°C
[density ]

1.271±0.06 g/cm3(Predicted)
[CAS DataBase Reference]

2674-91-1
[EPA Substance Registry System]

Oxydeprofos (2674-91-1)
Safety DataBack Directory
[RIDADR ]

3018
[HazardClass ]

6.1(a)
[PackingGroup ]

II
[Toxicity]

LD50 oral in rat: 89mg/kg
Hazard InformationBack Directory
[Uses]

ESP is an organophosphorus pesticide.
[Definition]

ChEBI:Oxydeprofos is a sulfoxide.
[Production Methods]

The industrial production process for oxydeprofos is not described in open literature. However, it can be inferred from its structure. It would typically begin with preparation of the O,O dimethyl phosphorothioate moiety, typically via chlorination of dimethyl phosphorothioic acid to form a reactive phosphoryl chloride intermediate. In parallel, the 2 (ethylsulfinyl)isopropyl thiol precursor would be generated by controlled oxidation of the corresponding thioether. These two fragments would then be coupled through S ester formation, producing the characteristic phosphorothioate–sulfoxide structure. After condensation, the crude material would be purified by washing and distillation to yield technical grade oxydeprofos
[Mechanism of action]

Systemic, contact action. Acetylcholinesterase (AchE) inhibitor.
[Pesticide Type]

Insecticide; Acaricide
Spectrum DetailBack Directory
[Spectrum Detail]

ESP(2674-91-1)MS
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