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Details

Stereochemistry ACHIRAL
Molecular Formula C15H11BrClF3N2O
Molecular Weight 407.613
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CHLORFENAPYR

SMILES

CCOCN1C(=C(C#N)C(Br)=C1C(F)(F)F)C2=CC=C(Cl)C=C2

InChI

InChIKey=CWFOCCVIPCEQCK-UHFFFAOYSA-N
InChI=1S/C15H11BrClF3N2O/c1-2-23-8-22-13(9-3-5-10(17)6-4-9)11(7-21)12(16)14(22)15(18,19)20/h3-6H,2,8H2,1H3

HIDE SMILES / InChI

Molecular Formula C15H11BrClF3N2O
Molecular Weight 407.613
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
A single gene (yes) controls pigmentation of eyes and scales in Heliothis virescens.
2001
Lethal and sublethal effects of insecticide residues on Orius insidiosus (Hemiptera: Anthocoridae) and Geocoris punctipes (Hemiptera: Lygaeidae).
2001 Feb
Efficacy of chlorfenapyr (AC 303630) experimental pour-on and CyLence formulations against naturally acquired louse infestations on cattle in New York.
2001 May 22
Chlorfenapyr resistance in two-spotted spider mite (Acari: Tetranychidae) from Australian cotton.
2004
Genetic analysis and cross-resistance spectrum of a laboratory-selected chlorfenapyr resistant strain of two-spotted spider mite (Acari: Tetranychidae).
2004
Fenpyroximate resistance in Tetranychus urticae (Acari: Tetranychidae): cross-resistance and biochemical resistance mechanisms.
2004 Oct
Synthesis and insecticidal activities of novel oxime ether pyrethroids.
2005 Feb
Dissipation of chlorfenapyr residue in pakchoi and soil.
2006 Dec
Laboratory evaluations of insecticide product efficacy for control of Cimex lectularius.
2006 Dec
[Toxicity of pesticides used in chrysanthemum crops to eggs and nymphs of Orius insidiosus (Say) (Hemiptera: Anthocoridae)].
2006 Jan-Feb
Mechanism and pathways of chlorfenapyr photocatalytic degradation in aqueous suspension of TiO2.
2006 May 15
Synthesis, insecticidal, and acaricidal activities of novel 2-aryl-pyrrole derivatives containing ester groups.
2008 Nov 12
Potential new insecticides for the control of western flower thrips (Thysanoptera: Thripidae) on sweet pepper, tomato, and lettuce.
2009 Apr
Control of pyrethroid-resistant Anopheles gambiae and Culex quinquefasciatus mosquitoes with chlorfenapyr in Benin.
2009 Apr
Determination of four heterocyclic insecticides by ionic liquid dispersive liquid-liquid microextraction in water samples.
2009 Feb 6
Behavioral responses of the bed bug to insecticide residues.
2009 Jan
Global status of DDT and its alternatives for use in vector control to prevent disease.
2009 Nov
Natural toxins for use in pest management.
2010 Aug
Toxicity of plant essential oils to acaricide-susceptible and -resistant Tetranychus urticae (Acari: Tetranychidae) and Neoseiulus californicus (Acari: Phytoseiidae).
2010 Aug
Optimization of odour-baited resting boxes for sampling malaria vector, Anopheles arabiensis Patton, in arid and highland areas of Africa.
2010 Aug 19
Control of subterranean termites (Isoptera: Rhinotermitidae) infesting power poles.
2010 Dec
[Selection of isolates of entomopathogenic fungi for controlling Tuta absoluta (Meyrick) (Lepidoptera: Gelechiidae) and their compatibility with insecticides used in tomato crop].
2010 Nov-Dec
Evaluation of indoor residual spraying with the pyrrole insecticide chlorfenapyr against pyrethroid-susceptible Anopheles arabiensis and pyrethroid-resistant Culex quinquefasciatus mosquitoes.
2010 Oct
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:35:43 GMT 2023
Edited
by admin
on Fri Dec 15 18:35:43 GMT 2023
Record UNII
NWI20P05EB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHLORFENAPYR
HSDB   ISO   MI  
Common Name English
CHLORFENAPYR [HSDB]
Common Name English
AC 303,630
Code English
AC-303630
Code English
4-BROMO-2-(4-CHLOROPHENYL)-1-(ETHOXYMETHYL)-5-(TRIFLUOROMETHYL)-1H-PYRROLE-3-CARBONITRILE
Systematic Name English
4-BROMO-2-(4-CHLOROPHENYL)-1-ETHOXYMETHYL-5-TRIFLUOROMETHYL-1H-PYRROLE-3-CARBONITRILE
Systematic Name English
CHLORFENAPYR [MI]
Common Name English
CHLORFENAPYR [ISO]
Common Name English
4-BROMO-2-(4-CHLOROPHENYL)-1-(ETHOXYMETHYL)-5(TRIFLUOROMETHYL)-1H-PYRROLE-3-CARBONITRILE
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 129093
Created by admin on Fri Dec 15 18:35:43 GMT 2023 , Edited by admin on Fri Dec 15 18:35:43 GMT 2023
Code System Code Type Description
ALANWOOD
chlorfenapyr
Created by admin on Fri Dec 15 18:35:43 GMT 2023 , Edited by admin on Fri Dec 15 18:35:43 GMT 2023
PRIMARY
FDA UNII
NWI20P05EB
Created by admin on Fri Dec 15 18:35:43 GMT 2023 , Edited by admin on Fri Dec 15 18:35:43 GMT 2023
PRIMARY
EPA CompTox
DTXSID9032533
Created by admin on Fri Dec 15 18:35:43 GMT 2023 , Edited by admin on Fri Dec 15 18:35:43 GMT 2023
PRIMARY
CAS
122453-73-0
Created by admin on Fri Dec 15 18:35:43 GMT 2023 , Edited by admin on Fri Dec 15 18:35:43 GMT 2023
PRIMARY
MERCK INDEX
m3359
Created by admin on Fri Dec 15 18:35:43 GMT 2023 , Edited by admin on Fri Dec 15 18:35:43 GMT 2023
PRIMARY Merck Index
PUBCHEM
91778
Created by admin on Fri Dec 15 18:35:43 GMT 2023 , Edited by admin on Fri Dec 15 18:35:43 GMT 2023
PRIMARY
WIKIPEDIA
CHLORFENAPYR
Created by admin on Fri Dec 15 18:35:43 GMT 2023 , Edited by admin on Fri Dec 15 18:35:43 GMT 2023
PRIMARY
HSDB
7464
Created by admin on Fri Dec 15 18:35:43 GMT 2023 , Edited by admin on Fri Dec 15 18:35:43 GMT 2023
PRIMARY
CHEBI
39347
Created by admin on Fri Dec 15 18:35:43 GMT 2023 , Edited by admin on Fri Dec 15 18:35:43 GMT 2023
PRIMARY
MESH
C436643
Created by admin on Fri Dec 15 18:35:43 GMT 2023 , Edited by admin on Fri Dec 15 18:35:43 GMT 2023
PRIMARY