| Identification | Back Directory | [Name]
FURALAXYL | [CAS]
57646-30-7 | [Synonyms]
a5430
fongani
FONGARID
cga38140
fonganil
FURALAXYL
Fongaride
furalaxyl (bsi,iso)
Furalaxyl Solution,100ppm
Furalaxyl @100 μg/mL in MeOH
TRIMETHYLTIN CHLORIDE PESTANAL, 250 MG
FURALAXYL PESTANAL (METHYL N-(2-FU- ROYL
Methyl N-(2-furoyl)-N-(2,6-xylyl)alaminate
METHYL N-(2-FUROYL)-N-(2,6-XYLYL)-DL-ALANINATE
n-(2-furoyl)-n-(2,6-xylyl)-,methylester,dl-alanin
methyln-(2,6-dimethylphenyl)-n-(2-furoyl)-dl-alaninate
methyl 2-[N-(furan-2-carbonyl)-2,6-dimethylanilino]propanoate
MethylN-(2,6-dimethylphenyl)-N-(2-furanyl-carbonyl)-alaninate
Methyl 2-(N-(2,6-diMethylphenyl)furan-2-carboxaMido)propanoate
methyl N-(2,6-dimethylphenyl)-N-(2-furylcarbonyl)-DL-alaninate
methyln-(2,6-dimethylphenyl)-n-(2-furanylcarbonyl)-dl-alaninate
N-(2,6-Dimethylphenyl)-N-(2-furanylcarbonyl)alanine methyl ester
n-(2,6-dimethylphenyl)-n-(2-furanylcarbonyl)-dl-alaninmethylester
Alanine, N-(2,6-dimethylphenyl)-N-(2-furanylcarbonyl)-, methyl ester
methyl N-(2,6-dimethylphenyl)-N-(2-furylcarbonyl)-DL-alaninate furalaxyl | [EINECS(EC#)]
260-875-1 | [Molecular Formula]
C17H19NO4 | [MDL Number]
MFCD00078674 | [MOL File]
57646-30-7.mol | [Molecular Weight]
301.34 |
| Chemical Properties | Back Directory | [Melting point ]
70℃ | [Boiling point ]
420.1±45.0 °C(Predicted) | [density ]
1.179±0.06 g/cm3(Predicted) | [vapor pressure ]
7 x 10-5 Pa (20 °C) | [form ]
neat | [pka]
1.35±0.50(Predicted) | [Water Solubility ]
230 mg l-1 (20 °C) | [BRN ]
6427785 |
| Hazard Information | Back Directory | [Uses]
Furalaxyl is used for the control of soil-borne diseases caused by
Phytophthora and Pythium species and other Oomycetes on ornamentals. | [Definition]
ChEBI: Methyl N-(2,6-dimethylphenyl)-N-2-furoylalaninate is an alanine derivative that is the N-furoyl derivative of methyl N-(2,6-dimethylphenyl)alaninate It is an alanine derivative, an aromatic amide, a carboxamide, a member of furans and a methyl ester. | [Origin]
Furalaxyl is a condensation product of furan-2-carboxylic acid and 2,6-dimethylaniline which is subsequently coupled with methyl 2-chloropropionate. The compound was introduced in 1984.
| [Metabolic pathway]
Incorporation of furalaxyl into the refreshed nutrient
solution is made several times at different plant growth
stages, and fulalaxyl is decomposed in the nutrient
solution into N-(2,6-dimethylphenyl-N-(2-
furanylcarbonyl)-DL-alanine and N-(2,6-
dimethylphenyl)-DL-alanine by an enzymatic process. | [Degradation]
Furalaxyl is a stable compound which is hydrolysed only at extreme pH
values. Its calculated DT50 values (20 °C) are, at pH 1, >200 days and at
pH 10,22 days (PM).
Furalaxyl was degraded when irradiated in aqueous solution with UV
light (254 nm) with a half-life of 86 minutes. This study used non-labelled
furalaxyl but the products of amide bond fission (2) and subsequent
N-dealkylation, 2,6-dimethylaniline (3) were identified (see Scheme
1). The product mixture was therefore simpler than that obtained for
metalaxyl under similar conditions. Under simulated sunlight conditions
degradation was slower with a half-life of 391 days (Pirisi et al., 1996). |
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