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Details

Stereochemistry RACEMIC
Molecular Formula C16H14Cl2O4
Molecular Weight 341.186
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DICLOFOP-METHYL

SMILES

COC(=O)C(C)OC1=CC=C(OC2=C(Cl)C=C(Cl)C=C2)C=C1

InChI

InChIKey=BACHBFVBHLGWSL-UHFFFAOYSA-N
InChI=1S/C16H14Cl2O4/c1-10(16(19)20-2)21-12-4-6-13(7-5-12)22-15-8-3-11(17)9-14(15)18/h3-10H,1-2H3

HIDE SMILES / InChI

Molecular Formula C16H14Cl2O4
Molecular Weight 341.186
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Two complementary bioassays for screening the estrogenic potency of xenobiotics: recombinant yeast for trout estrogen receptor and trout hepatocyte cultures.
1997 Dec
Comparative efficacy of five herbicides on winter cereal weeds in semi-arid region of Algeria.
2001
Studies of early hepatocellular proliferation and peroxisomal proliferation in Wistar rats treated with herbicide diclofop.
2001 Feb 14
Resistance to ACCase-inhibiting herbicides and isoproturon in UK populations of Lolium multiflorum: mechanisms of resistance and implications for control.
2001 Jul
Effect of cropping cycles and repeated herbicide applications on the degradation of diclofop-methyl, bentazone, diuron, isoproturon and pendimethalin in soil.
2002 Mar
PCR-based detection of resistance to acetyl-CoA carboxylase-inhibiting herbicides in black-grass (Alopecurus myosuroides Huds) and ryegrass (Lolium rigidum gaud).
2002 May
Cross-resistance to ACCase inhibitors of Lolium multiflorum, Lolium perenne and Lolium rigidum found in Chile.
2003
Tank-mix adjuvants and pesticide residues: some regulatory and quantitative aspects.
2003 Nov
Cross resistance to accase herbicide in Lolium rigidum.
2004
Determination of commonly used herbicides in surface water using solid-phase extraction and dual-column HPLC-DAD.
2005
Effects of methyl-CD and humic acid on hydrolytic degradation of the herbicide diclofop-methyl.
2005
Recurrent selection with reduced herbicide rates results in the rapid evolution of herbicide resistance in Lolium rigidum.
2005 Apr
Environmental effects of inclusion complexation between methylated beta-cyclodextrin and diclofop-methyl.
2005 Aug 24
High survival frequencies at low herbicide use rates in populations of Lolium rigidum result in rapid evolution of herbicide resistance.
2005 Dec
Lolium rigidum, a pool of resistance mechanisms to ACCase inhibitor herbicides.
2005 Mar 23
Bioluminescence determination of enzyme activity of firefly luciferase in the presence of pesticides.
2005 May-Jun
Environmental significance of the diclofop-methyl and cyclodextrin inclusion complexes.
2006
Enantiomeric resolution of chiral pesticides by high-performance liquid chromatography.
2006 Mar 8
Agricultural pesticide use and hypospadias in eastern Arkansas.
2006 Oct
Relation of diclofop-methyl toxicity and degradation in algae cultures.
2007 May
One- and two-dimensional direct chiral liquid chromatographic determination of mixtures of diclofop-Acid and diclofop-methyl herbicides.
2008 Apr 9
Enantioselective degradation and ecotoxicity of the chiral herbicide diclofop in three freshwater alga cultures.
2008 Mar 26
TiO(2)/BaTiO(3)-assisted photocatalytic mineralization of diclofop-methyl on UV-light irradiation in the presence of oxidizing agents.
2009 Mar 15
Chemical control of herbicide-resistant Lolium rigidum Gaud. in north-eastern Spain.
2010 Dec
Environmental behavior of the chiral aryloxyphenoxypropionate herbicide diclofop-methyl and diclofop: enantiomerization and enantioselective degradation in soil.
2010 Mar 15
Impact of environmental chemicals on key transcription regulators and correlation to toxicity end points within EPA's ToxCast program.
2010 Mar 15
An aspartate to glycine change in the carboxyl transferase domain of acetyl CoA carboxylase and non-target-site mechanism(s) confer resistance to ACCase inhibitor herbicides in a Lolium multiflorum population.
2010 Nov
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:32:51 GMT 2023
Edited
by admin
on Sat Dec 16 08:32:51 GMT 2023
Record UNII
9T8QCB25UO
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DICLOFOP-METHYL
ISO   MI  
Common Name English
AVENOXAN
Brand Name English
DICHLORFOP-METHYL
HSDB  
Common Name English
DICHLORFOP-METHYL [HSDB]
Common Name English
PROPANOIC ACID, 2-(4-(2,4-DICHLOROPHENOXY)PHENOXY)-, METHYL ESTER
Systematic Name English
ILLOXAN
Common Name English
HOELON
Common Name English
METHYL DICLOFOP
Common Name English
2-(4-(2,4-DICHLOROPHENOXY)PHENOXY)PROPANOIC ACID, METHYL ESTER
Systematic Name English
DICLOFOP-METHYL [ISO]
Common Name English
HOEGRASS
Common Name English
METHYL 2-(4-(2,4-DICHLOROPHENOXY)PHENOXY)PROPANOATE
Systematic Name English
DICHLORDIPHENPROP
Common Name English
METHYL 2-(4-(2,4-DICHLOROPHENOXY)PHENOXY)PROPIONATE
Systematic Name English
METHYLDICLOFOP
Common Name English
DICLOFOP-METHYL [MI]
Common Name English
DICLOFOP-METHYL, (±)-
Systematic Name English
DICLOFOP METHYL
Common Name English
DICLOFOP METHYL ESTER
Common Name English
DICLOSAN
Common Name English
METHYL 2-(4-(2,4-DICHLOROPHENOXY)PHENOXY)PROPIONATE, (±)-
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 110902
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
Code System Code Type Description
ALANWOOD
diclofop-methyl
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY
HSDB
6607
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY
FDA UNII
9T8QCB25UO
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY
CAS
51338-27-3
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY
MERCK INDEX
m4362
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY Merck Index
DRUG BANK
DB13918
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY
ECHA (EC/EINECS)
257-141-8
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY
CHEBI
4510
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY
EPA CompTox
DTXSID0032605
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY
PUBCHEM
39985
Created by admin on Sat Dec 16 08:32:51 GMT 2023 , Edited by admin on Sat Dec 16 08:32:51 GMT 2023
PRIMARY