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Details

Stereochemistry ACHIRAL
Molecular Formula C9H11Cl2O3PS
Molecular Weight 301.127
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TOLCLOFOS-METHYL

SMILES

COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl

InChI

InChIKey=OBZIQQJJIKNWNO-UHFFFAOYSA-N
InChI=1S/C9H11Cl2O3PS/c1-6-4-7(10)9(8(11)5-6)14-15(16,12-2)13-3/h4-5H,1-3H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparative study of human and mouse pregnane X receptor agonistic activity in 200 pesticides using in vitro reporter gene assays.
2011-02-27
Monitoring of pesticide residues in vegetables marketed in Al-Qassim region, Saudi Arabia.
2010-09
Fungicide-driven evolution and molecular basis of multidrug resistance in field populations of the grey mould fungus Botrytis cinerea.
2009-12
Effects of chlorine on organophosphorus pesticides adsorbed on activated carbon: desorption and oxon formation.
2008-03
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Evaluation of the estrogenic activities of some pesticides and their combinations using MtT/Se cell proliferation assay.
2006-09
Effect of pesticides on estrogen receptor transactivation in vitro: a comparison of stable transfected MVLN and transient transfected MCF-7 cells.
2005-12-01
Evaluation of estrogenic activities of pesticides using an in vitro reporter gene assay.
2005-08
Screening for estrogen and androgen receptor activities in 200 pesticides by in vitro reporter gene assays using Chinese hamster ovary cells.
2004-04
Interactions between nematophagous fungi and consequences for their potential as biological agents for the control of potato cyst nematodes.
2003-01
Monitoring of five postharvest fungicides in fruit and vegetables by matrix solid-phase dispersion and liquid chromatography/mass spectrometry.
2002-06-27
Effects of currently used pesticides in assays for estrogenicity, androgenicity, and aromatase activity in vitro.
2002-02-15
Evaluation of respiratory and cutaneous doses and urinary excretion of alkylphosphates by workers in greenhouses treated with omethoate, fenitrothion, and tolclofos-methyl.
2001-03-22
Patents
Name Type Language
TOLCLOFOS-METHYL
ISO   MI  
Common Name English
RIZOLEX
Preferred Name English
TOLCLOFOS-METHYL [ISO]
Common Name English
O-(2,6-DICHLORO-4-METHYLPHENYL) O,O-DIMETHYL PHOSPHOROTHIOATE
Systematic Name English
O-2,6-DICHLORO-P-TOLYL O,O-DIMETHYL PHOSPHOROTHIOATE
Common Name English
TOLCLOFOS-METHYL [MI]
Common Name English
S-3349
Code English
Classification Tree Code System Code
EPA PESTICIDE CODE 128905
Created by admin on Mon Mar 31 19:07:42 GMT 2025 , Edited by admin on Mon Mar 31 19:07:42 GMT 2025
Code System Code Type Description
MESH
C426783
Created by admin on Mon Mar 31 19:07:42 GMT 2025 , Edited by admin on Mon Mar 31 19:07:42 GMT 2025
PRIMARY
ALANWOOD
tolclofos-methyl
Created by admin on Mon Mar 31 19:07:42 GMT 2025 , Edited by admin on Mon Mar 31 19:07:42 GMT 2025
PRIMARY
MERCK INDEX
m10940
Created by admin on Mon Mar 31 19:07:42 GMT 2025 , Edited by admin on Mon Mar 31 19:07:42 GMT 2025
PRIMARY Merck Index
PUBCHEM
91664
Created by admin on Mon Mar 31 19:07:42 GMT 2025 , Edited by admin on Mon Mar 31 19:07:42 GMT 2025
PRIMARY
ECHA (EC/EINECS)
260-515-3
Created by admin on Mon Mar 31 19:07:42 GMT 2025 , Edited by admin on Mon Mar 31 19:07:42 GMT 2025
PRIMARY
CAS
57018-04-9
Created by admin on Mon Mar 31 19:07:42 GMT 2025 , Edited by admin on Mon Mar 31 19:07:42 GMT 2025
PRIMARY
CHEBI
81731
Created by admin on Mon Mar 31 19:07:42 GMT 2025 , Edited by admin on Mon Mar 31 19:07:42 GMT 2025
PRIMARY
EPA CompTox
DTXSID0034776
Created by admin on Mon Mar 31 19:07:42 GMT 2025 , Edited by admin on Mon Mar 31 19:07:42 GMT 2025
PRIMARY
FDA UNII
G42OQL6F5B
Created by admin on Mon Mar 31 19:07:42 GMT 2025 , Edited by admin on Mon Mar 31 19:07:42 GMT 2025
PRIMARY