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Details

Stereochemistry ACHIRAL
Molecular Formula C14H9Cl2NO5
Molecular Weight 342.131
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BIFENOX

SMILES

COC(=O)C1=CC(OC2=CC=C(Cl)C=C2Cl)=CC=C1[N+]([O-])=O

InChI

InChIKey=SUSRORUBZHMPCO-UHFFFAOYSA-N
InChI=1S/C14H9Cl2NO5/c1-21-14(18)10-7-9(3-4-12(10)17(19)20)22-13-5-2-8(15)6-11(13)16/h2-7H,1H3

HIDE SMILES / InChI

Molecular Formula C14H9Cl2NO5
Molecular Weight 342.131
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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
[Determination of biphenyl ether herbicides in water using HPLC with cloud-point extraction].
2010-01
Utility of delayed fluorescence as endpoint for rapid estimation of effect concentration on the green alga Pseudokirchneriella subcapitata.
2009-10
In vitro screening for aryl hydrocarbon receptor agonistic activity in 200 pesticides using a highly sensitive reporter cell line, DR-EcoScreen cells, and in vivo mouse liver cytochrome P450-1A induction by propanil, diuron and linuron.
2008-12
Combining ligand-based pharmacophore modeling, quantitative structure-activity relationship analysis and in silico screening for the discovery of new potent hormone sensitive lipase inhibitors.
2008-10-23
Screening of 397 chemicals and development of a quantitative structure--activity relationship model for androgen receptor antagonism.
2008-04
Determination of diphenylether herbicides in water samples by solid-phase microextraction coupled to liquid chromatography.
2006-11
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Double-layer effects and distance dependence of electron transfer in reduction of nitro aromatic radical anions.
2006-02-14
Screening for estrogen and androgen receptor activities in 200 pesticides by in vitro reporter gene assays using Chinese hamster ovary cells.
2004-04
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:41:31 GMT 2025
Edited
by admin
on Mon Mar 31 18:41:31 GMT 2025
Record UNII
KSB85XT26Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MODOWN
Preferred Name English
BIFENOX
HSDB   ISO   MI  
Common Name English
5-(2,4-DICHLOROPHENOXY)-2-NITROBENZOIC ACID METHYL ESTER
Systematic Name English
MC-4379
Common Name English
BIFENOX [MI]
Common Name English
METHYL 5-(2,4-DICHLOROPHENOXY)-2-NITROBENZOATE
Systematic Name English
BIFENOX [HSDB]
Common Name English
2,4-DICHLOROPHENYL 3-(METHOXYCARBONYL)-4-NITROPHENYL ETHER
Systematic Name English
BIFENOX [ISO]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 104301
Created by admin on Mon Mar 31 18:41:31 GMT 2025 , Edited by admin on Mon Mar 31 18:41:31 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID1040320
Created by admin on Mon Mar 31 18:41:31 GMT 2025 , Edited by admin on Mon Mar 31 18:41:31 GMT 2025
PRIMARY
PUBCHEM
39230
Created by admin on Mon Mar 31 18:41:31 GMT 2025 , Edited by admin on Mon Mar 31 18:41:31 GMT 2025
PRIMARY
WIKIPEDIA
Bifenox
Created by admin on Mon Mar 31 18:41:31 GMT 2025 , Edited by admin on Mon Mar 31 18:41:31 GMT 2025
PRIMARY
CAS
42576-02-3
Created by admin on Mon Mar 31 18:41:31 GMT 2025 , Edited by admin on Mon Mar 31 18:41:31 GMT 2025
PRIMARY
FDA UNII
KSB85XT26Y
Created by admin on Mon Mar 31 18:41:31 GMT 2025 , Edited by admin on Mon Mar 31 18:41:31 GMT 2025
PRIMARY
MERCK INDEX
m2482
Created by admin on Mon Mar 31 18:41:31 GMT 2025 , Edited by admin on Mon Mar 31 18:41:31 GMT 2025
PRIMARY Merck Index
HSDB
6567
Created by admin on Mon Mar 31 18:41:31 GMT 2025 , Edited by admin on Mon Mar 31 18:41:31 GMT 2025
PRIMARY
ECHA (EC/EINECS)
255-894-7
Created by admin on Mon Mar 31 18:41:31 GMT 2025 , Edited by admin on Mon Mar 31 18:41:31 GMT 2025
PRIMARY
ALANWOOD
bifenox
Created by admin on Mon Mar 31 18:41:31 GMT 2025 , Edited by admin on Mon Mar 31 18:41:31 GMT 2025
PRIMARY