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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
Screening for estrogen and androgen receptor activities in 200 pesticides by in vitro reporter gene assays using Chinese hamster ovary cells.
2004 Apr
Determination of diphenylether herbicides in water samples by solid-phase microextraction coupled to liquid chromatography.
2006 Nov
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006 Nov
Screening of 397 chemicals and development of a quantitative structure--activity relationship model for androgen receptor antagonism.
2008 Apr
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 Dec
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 Oct 23
Utility of delayed fluorescence as endpoint for rapid estimation of effect concentration on the green alga Pseudokirchneriella subcapitata.
2009 Oct
[Determination of biphenyl ether herbicides in water using HPLC with cloud-point extraction].
2010 Jan
Comparative study of human and mouse pregnane X receptor agonistic activity in 200 pesticides using in vitro reporter gene assays.
2011 Feb 27
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:10:45 GMT 2023
Edited
by admin
on Fri Dec 15 17:10:45 GMT 2023
Record UNII
KSB85XT26Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BIFENOX
HSDB   ISO   MI  
Common Name English
5-(2,4-DICHLOROPHENOXY)-2-NITROBENZOIC ACID METHYL ESTER
Systematic Name English
MODOWN
Brand 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 Fri Dec 15 17:10:45 GMT 2023 , Edited by admin on Fri Dec 15 17:10:45 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID1040320
Created by admin on Fri Dec 15 17:10:45 GMT 2023 , Edited by admin on Fri Dec 15 17:10:45 GMT 2023
PRIMARY
PUBCHEM
39230
Created by admin on Fri Dec 15 17:10:45 GMT 2023 , Edited by admin on Fri Dec 15 17:10:45 GMT 2023
PRIMARY
WIKIPEDIA
Bifenox
Created by admin on Fri Dec 15 17:10:45 GMT 2023 , Edited by admin on Fri Dec 15 17:10:45 GMT 2023
PRIMARY
CAS
42576-02-3
Created by admin on Fri Dec 15 17:10:45 GMT 2023 , Edited by admin on Fri Dec 15 17:10:45 GMT 2023
PRIMARY
FDA UNII
KSB85XT26Y
Created by admin on Fri Dec 15 17:10:45 GMT 2023 , Edited by admin on Fri Dec 15 17:10:45 GMT 2023
PRIMARY
MERCK INDEX
m2482
Created by admin on Fri Dec 15 17:10:45 GMT 2023 , Edited by admin on Fri Dec 15 17:10:45 GMT 2023
PRIMARY Merck Index
HSDB
6567
Created by admin on Fri Dec 15 17:10:45 GMT 2023 , Edited by admin on Fri Dec 15 17:10:45 GMT 2023
PRIMARY
ECHA (EC/EINECS)
255-894-7
Created by admin on Fri Dec 15 17:10:45 GMT 2023 , Edited by admin on Fri Dec 15 17:10:45 GMT 2023
PRIMARY
ALANWOOD
bifenox
Created by admin on Fri Dec 15 17:10:45 GMT 2023 , Edited by admin on Fri Dec 15 17:10:45 GMT 2023
PRIMARY