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Details

Stereochemistry RACEMIC
Molecular Formula C17H13ClFN3O
Molecular Weight 329.756
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EPOXICONAZOLE

SMILES

FC1=CC=C(C=C1)[C@@]3(CN2C=NC=N2)O[C@@H]3C4=C(Cl)C=CC=C4

InChI

InChIKey=ZMYFCFLJBGAQRS-IAGOWNOFSA-N
InChI=1S/C17H13ClFN3O/c18-15-4-2-1-3-14(15)16-17(23-16,9-22-11-20-10-21-22)12-5-7-13(19)8-6-12/h1-8,10-11,16H,9H2/t16-,17-/m1/s1

HIDE SMILES / InChI
Molecular Formula C17H13ClFN3O
Molecular Weight 329.756
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Description

Epoxiconazole is a broad-spectrum fungicide, with preventive and curative action, for control of diseases caused by Ascomycetes, Basidiomycetes, and Deuteromycetes in cereals, sugar beet, peanuts, oilseed rape, and ornamentals. It induces ROS generation, lipid peroxidation and DNA damage in mammals both in vitro and in vivo.

Approval Year

Unknown
149124
Patents

Patents

JP2011246452A
8
JP2011509959A
61
JP2011511032A
40
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:05:06 GMT 2025
Edited
by admin
on Mon Mar 31 21:05:06 GMT 2025
Record UNII
U80T84L776
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OPAL
Preferred Name English
EPOXICONAZOLE
ISO   MI  
Common Name English
1H-1,2,4-TRIAZOLE, 1-((3-(2-CHLOROPHENYL)-2-(4-FLUOROPHENYL)OXIRANYL)METHYL)-, CIS-(±)-
Systematic Name English
EPOXICONAZOLE [ISO]
Common Name English
(2RS,3RS)-1-(3-(2-CHLOROPHENYL)-2,3-EPOXY-2-(4-FLUOROPHENYL)-PROPYL)-1H-1,2,4-TRIAZOLE
Systematic Name English
EPOXICONAZOLE [MI]
Common Name English
1H-1,2,4-TRIAZOLE, 1-(((2R,3S)-3-(2-CHLOROPHENYL)-2-(4-FLUOROPHENYL)-2-OXIRANYL)METHYL)-, REL-
Systematic Name English
BAS-480-F
Code English
OPUS
Brand Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 123909
Created by admin on Mon Mar 31 21:05:06 GMT 2025 , Edited by admin on Mon Mar 31 21:05:06 GMT 2025
Code System Code Type Description
PUBCHEM
107901
Created by admin on Mon Mar 31 21:05:06 GMT 2025 , Edited by admin on Mon Mar 31 21:05:06 GMT 2025
PRIMARY
CAS
106325-08-0
Created by admin on Mon Mar 31 21:05:06 GMT 2025 , Edited by admin on Mon Mar 31 21:05:06 GMT 2025
SUPERSEDED
DAILYMED
U80T84L776
Created by admin on Mon Mar 31 21:05:06 GMT 2025 , Edited by admin on Mon Mar 31 21:05:06 GMT 2025
PRIMARY
FDA UNII
U80T84L776
Created by admin on Mon Mar 31 21:05:06 GMT 2025 , Edited by admin on Mon Mar 31 21:05:06 GMT 2025
PRIMARY
ALANWOOD
epoxiconazole
Created by admin on Mon Mar 31 21:05:06 GMT 2025 , Edited by admin on Mon Mar 31 21:05:06 GMT 2025
PRIMARY
CAS
133855-98-8
Created by admin on Mon Mar 31 21:05:06 GMT 2025 , Edited by admin on Mon Mar 31 21:05:06 GMT 2025
PRIMARY
SMS_ID
300000052897
Created by admin on Mon Mar 31 21:05:06 GMT 2025 , Edited by admin on Mon Mar 31 21:05:06 GMT 2025
PRIMARY
MERCK INDEX
m4955
Created by admin on Mon Mar 31 21:05:06 GMT 2025 , Edited by admin on Mon Mar 31 21:05:06 GMT 2025
PRIMARY Merck Index
RXCUI
2593180
Created by admin on Mon Mar 31 21:05:06 GMT 2025 , Edited by admin on Mon Mar 31 21:05:06 GMT 2025
PRIMARY
EPA CompTox
DTXSID1040372
Created by admin on Mon Mar 31 21:05:06 GMT 2025 , Edited by admin on Mon Mar 31 21:05:06 GMT 2025
PRIMARY
CHEBI
64389
Created by admin on Mon Mar 31 21:05:06 GMT 2025 , Edited by admin on Mon Mar 31 21:05:06 GMT 2025
PRIMARY
NIH
NCATS
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