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Details

Stereochemistry RACEMIC
Molecular Formula C14H16Cl3NO2
Molecular Weight 336.641
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ZOXAMIDE

SMILES

CCC(C)(NC(=O)C1=CC(Cl)=C(C)C(Cl)=C1)C(=O)CCl

InChI

InChIKey=SOUGWDPPRBKJEX-UHFFFAOYSA-N
InChI=1S/C14H16Cl3NO2/c1-4-14(3,12(19)7-15)18-13(20)9-5-10(16)8(2)11(17)6-9/h5-6H,4,7H2,1-3H3,(H,18,20)

HIDE SMILES / InChI

Molecular Formula C14H16Cl3NO2
Molecular Weight 336.641
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Environmental impact on vascular development predicted by high-throughput screening.
2011-11
Baseline sensitivity and resistance-risk assessment of Phytophthora capsici to iprovalicarb.
2010-11
In vitro mammalian metabolism of the mitosis inhibitor zoxamide and the relationship to its in vitro toxicity.
2010-01
Multiresidue determination of 11 new fungicides in grapes and wines by liquid-liquid extraction/clean-up and programmable temperature vaporization injection with analyte protectants/gas chromatography/ion trap mass spectrometry.
2009-08-07
Chemical control of downy mildew on lettuce and basil under greenhouse.
2009
Statistical study of the influence of fungicide treatments (mancozeb, zoxamide and copper oxychloride) on heavy metal concentrations in Sicilian red wine.
2008-03
Approach for extrapolating in vitro metabolism data to refine bioconcentration factor estimates.
2008-02
Gas chromatographic ion trap mass spectrometry determination of zoxamide residues in grape, grape processing, and in the fermentation process.
2005-12-02
Evaluation of fungicides for the control of carrot cavity spot.
2005-08
Preparative-scale synthesis of two metabolites isolated from soil treated with zoxium fungicide and kerb herbicide.
2002-01-30
Laboratory studies to assess the risk of development of resistance to zoxamide.
2001-11
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:20:54 GMT 2025
Edited
by admin
on Mon Mar 31 22:20:54 GMT 2025
Record UNII
F1XZW465PC
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ZOXIUM
HSDB  
Preferred Name English
ZOXAMIDE
ISO   MI  
Common Name English
ZOXAMIDE [ISO]
Common Name English
3,5-DICHLORO-N-(3-CHLORO-1-ETHYL-1-METHYL-2-OXOPROPYL)-4- METHYLBENZAMIDE
Systematic Name English
3,5-DICHLORO-N-(3-CHLORO-1-ETHYL-1-METHYL-2-OXOPROPYL)-P- TOLUAMIDE
Common Name English
RH-7281
Code English
BENZAMIDE, 3,5-DICHLORO-N-(3-CHLORO-1-ETHYL-1-METHYL-2- OXOPROPYL)-4-METHYL-
Systematic Name English
ZOXAMIDE [MI]
Common Name English
ZOXIUM [HSDB]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 101702
Created by admin on Mon Mar 31 22:20:54 GMT 2025 , Edited by admin on Mon Mar 31 22:20:54 GMT 2025
Code System Code Type Description
FDA UNII
F1XZW465PC
Created by admin on Mon Mar 31 22:20:54 GMT 2025 , Edited by admin on Mon Mar 31 22:20:54 GMT 2025
PRIMARY
EPA CompTox
DTXSID9032581
Created by admin on Mon Mar 31 22:20:54 GMT 2025 , Edited by admin on Mon Mar 31 22:20:54 GMT 2025
PRIMARY
MERCK INDEX
m11668
Created by admin on Mon Mar 31 22:20:54 GMT 2025 , Edited by admin on Mon Mar 31 22:20:54 GMT 2025
PRIMARY Merck Index
PUBCHEM
122087
Created by admin on Mon Mar 31 22:20:54 GMT 2025 , Edited by admin on Mon Mar 31 22:20:54 GMT 2025
PRIMARY
CAS
156052-68-5
Created by admin on Mon Mar 31 22:20:54 GMT 2025 , Edited by admin on Mon Mar 31 22:20:54 GMT 2025
PRIMARY
HSDB
7278
Created by admin on Mon Mar 31 22:20:54 GMT 2025 , Edited by admin on Mon Mar 31 22:20:54 GMT 2025
PRIMARY
ALANWOOD
zoxamide
Created by admin on Mon Mar 31 22:20:54 GMT 2025 , Edited by admin on Mon Mar 31 22:20:54 GMT 2025
PRIMARY