BIFENOX

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 Search

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

Title	Date	PubMed
Screening for estrogen and androgen receptor activities in 200 pesticides by in vitro reporter gene assays using Chinese hamster ovary cells.	2004 Apr	15064155
Double-layer effects and distance dependence of electron transfer in reduction of nitro aromatic radical anions.	2006 Feb 14	16460125
Determination of diphenylether herbicides in water samples by solid-phase microextraction coupled to liquid chromatography.	2006 Nov	17313105
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.	2006 Nov	16497524
Screening of 397 chemicals and development of a quantitative structure--activity relationship model for androgen receptor antagonism.	2008 Apr	18324785
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	18835618
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	18808096
Utility of delayed fluorescence as endpoint for rapid estimation of effect concentration on the green alga Pseudokirchneriella subcapitata.	2009 Oct	19629368
[Determination of biphenyl ether herbicides in water using HPLC with cloud-point extraction].	2010 Jan	20369492
Comparative study of human and mouse pregnane X receptor agonistic activity in 200 pesticides using in vitro reporter gene assays.	2011 Feb 27	21115097

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

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Name

Type

Language

BIFENOX

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