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103112-35-2

103112-35-2 Structure

103112-35-2 Structure
IdentificationBack Directory
[Name]

FENCHLORAZOL-ETHYL
[CAS]

103112-35-2
[Synonyms]

hoe070542
fenchlorazole-et
FENCHLORAZOL-ETHYL
fenchlorazole-ethyl
fenchlorazole-ethyl (bsi,draft e-iso)
ethyl1-(2,4-dichlorophenyl)-5-(trichloromethyl)-1h-1,2,4-triazole-3-carboxyl
1h-1,2,4-triazole-3-carboxylicacid,1-(2,4-dichlorophenyl)-5-(trichloromethyl)
ETHYL 1-(2,4-DICHLOROPHENYL)-5-(TRICHLOROMETHYL)-1H-1,2,4-TRIAZOLE-3-CARBOXYLATE
1-(2,4-Dichlorophenyl)-5-(trichloromethyl)-1H-1,2,4-triazole-3-carboxylic acid ethyl ester
1H-1,2,4-Triazole-3-carboxylic acid, 1-(2,4-dichlorophenyl)-5-(trichloromethyl)-, ethyl ester
Fenchlorazol-ethyl,Ethyl 1-(2,4-dichlorophenyl)-5-(trichloromethyl)-1H-1,2,4-triazole-3-carboxylate,
[EINECS(EC#)]

401-290-5
[Molecular Formula]

C12H8Cl5N3O2
[MDL Number]

MFCD02101622
[MOL File]

103112-35-2.mol
[Molecular Weight]

403.48
Chemical PropertiesBack Directory
[Melting point ]

110 °C
[Boiling point ]

469.8±55.0 °C(Predicted)
[density ]

1.65±0.1 g/cm3(Predicted)
[form ]

neat
[pka]

-3.59±0.50(Predicted)
[Henry's Law Constant]

2.7×103 mol/(m3Pa) at 25℃, MacBean (2012)
[EPA Substance Registry System]

1H-1,2,4-Triazole-3-carboxylic acid, 1-(2,4-dichlorophenyl)-5-(trichloromethyl)-, ethyl ester (103112-35-2)
Safety DataBack Directory
[Hazard Codes ]

T,N
[Risk Statements ]

45-50/53
[Safety Statements ]

53-45-60-61
[RIDADR ]

UN3077 9/PG 3
[WGK Germany ]

3
[RTECS ]

XZ4272500
[REACH Registrations]

Inactive
[HS Code ]

29339900
Hazard InformationBack Directory
[Chemical Properties]

Antiflorazole is white odorless solid, melting point 108~112℃, vapor pressure 8.9×10-4mPa(20℃).Henry's constant 3.71×10-4 Pa-m3/mol(20℃, calculated value). Relative density 1.7(20℃). Solubility in water 0.9mg/L(20℃,pH4.5). Solubility in organic solvents (20℃ ,g/L): acetone 360, dichloromethane ≥500, n-hexane 2.5, methanol 27, toluene 270.Hydrolysis in aqueous solution DT50: 115d (pH 5), 5.5d (pH 7), 0.079d (pH 9).
[Uses]

Field trials of FENCHLORAZOL-ETHYL under various climatic and agricultural conditions have demonstrated its high herbicidal activity against many grassy weeds, including Alopecurus aegypti, oats, sedge, and purslane. When used to control grassy weeds, it does not affect the herbicidal activity of quizalofop-p-ethyl. It exhibits no herbicidal activity whether applied pre-emergence or post-emergence, even at dosages as high as 10 kg/hm².
[Definition]

ChEBI: Fenchlorazole-ethyl is a dichlorobenzene.
[Synthesis]

Fenchlorazol-ethyl can be synthesized by reacting Ethyl 2-[2-(2,4-dichlorophenyl)hydrazinyl]-2-iminoacetate with 2,2,2-Trichloroacetyl chloride. The solvent used is Toluene.
synthesis of FENCHLORAZOL-ETHYL
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