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Details

Stereochemistry ACHIRAL
Molecular Formula C12H18O4S2
Molecular Weight 290.399
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ISOPROTHIOLANE

SMILES

CC(C)OC(=O)C(C(=O)OC(C)C)=C1SCCS1

InChI

InChIKey=UFHLMYOGRXOCSL-UHFFFAOYSA-N
InChI=1S/C12H18O4S2/c1-7(2)15-10(13)9(11(14)16-8(3)4)12-17-5-6-18-12/h7-8H,5-6H2,1-4H3

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
Pesticide residues in soils, sediments, and vegetables in the Red River Delta, northern Vietnam.
2010-10
Synthesis, fungicidal activity, and structure-activity relationship of spiro-compounds containing macrolactam (macrolactone) and thiadiazoline rings.
2010-03-10
Sensitivity analysis using a diffuse pollution hydrologic model to assess factors affecting pesticide concentrations in river water.
2010
Toxicity of agricultural chemicals in Daphnia magna.
2009-12
Daily variation of pesticides in surface water of a small river flowing through paddy field area.
2009-06
Pesticides in water and sediment from littoral area of Lake Biwa.
2009-06
Development and validation of a multiresidue method for determination of 82 pesticides in water using GC.
2009-02
Evaluation of pressurized liquid extraction for the analysis of four pesticides in unpolished rice.
2008-06
Potential of Trichoderma species on Helminthosporium causing leaf spot on cane palm, Chrysalidocarpus lutescens.
2008
Simple one-step extraction and cleanup by pressurized liquid extraction for gas chromatographic-mass spectrometric determination of pesticides in green leafy vegetables.
2007-12-21
Investigation of the estrogenic activities of pesticides from Pal-dang reservoir by in vitro assay.
2007-12-15
A multiresidue method for the analysis of pesticide residues in polished rice (Oryza sativa L.) using accelerated solvent extraction and gas chromatography and confirmation by mass spectrometry.
2007-06
Assessment of human pregnane X receptor involvement in pesticide-mediated activation of CYP3A4 gene.
2007-05
Using precise data sets on farming and pesticide properties to verify a diffuse pollution hydrological model for predicting pesticide concentration.
2007
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Molluscicidal effect of fungicide, herbicide and plant extract on some biological and physiological parameters of Biomphalaria alexandrina.
2002-12
Molluscicidal activities of certain pesticide and their mixtures against Biomphalaria alexandrina.
2002-04
Prognostic significance of nonsustained ventricular tachycardia after revascularization.
2002-04
Concentration and loading of pesticide residues in Lake Biwa basin (Japan).
2002-01
Nitrate and pesticide removal by a combined bioelectrochemical/adsorption process.
2001
Patents
Name Type Language
ISOPROTHIOLANE
ISO  
Common Name English
FUJI-ONE
Preferred Name English
DI(PROPAN-2-YL) 1,3-DITHIOLAN-2-YLIDENEMALONATE
Systematic Name English
PROPANEDIOIC ACID, 2-(1,3-DITHIOLAN-2-YLIDENE)-, BIS(1-METHYLETHYL) ESTER
Common Name English
NKK 100
Code English
BIS(1-METHYLETHYL) 1,3-DITHIOLAN-2-YLIDENEPROPANEDIOATE
Systematic Name English
DIISOPROPYL 1,3-DITHIOLAN-2-YLIDENEMALONATE
Systematic Name English
PROPANEDIOIC ACID, 1,3-DITHIOLAN-2-YLIDENE-, BIS(1-METHYLETHYL) ESTER
Common Name English
NNF 109
Code English
ISOPROTHIOLANE [ISO]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 68300
Created by admin on Mon Mar 31 18:47:59 GMT 2025 , Edited by admin on Mon Mar 31 18:47:59 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID8058110
Created by admin on Mon Mar 31 18:47:59 GMT 2025 , Edited by admin on Mon Mar 31 18:47:59 GMT 2025
PRIMARY
PUBCHEM
39681
Created by admin on Mon Mar 31 18:47:59 GMT 2025 , Edited by admin on Mon Mar 31 18:47:59 GMT 2025
PRIMARY
ALANWOOD
isoprothiolane
Created by admin on Mon Mar 31 18:47:59 GMT 2025 , Edited by admin on Mon Mar 31 18:47:59 GMT 2025
PRIMARY
CAS
50512-35-1
Created by admin on Mon Mar 31 18:47:59 GMT 2025 , Edited by admin on Mon Mar 31 18:47:59 GMT 2025
PRIMARY
FDA UNII
88HCS898G6
Created by admin on Mon Mar 31 18:47:59 GMT 2025 , Edited by admin on Mon Mar 31 18:47:59 GMT 2025
PRIMARY
CHEBI
6047
Created by admin on Mon Mar 31 18:47:59 GMT 2025 , Edited by admin on Mon Mar 31 18:47:59 GMT 2025
PRIMARY