Difenoconazole

  • CasNo:119446-68-3
  • Purity:
  • Molecular Formula:C19H17Cl2N3O3
  • Molecular Weight:406.268
  • Melting Point: 76 °C 
  • Apply:
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Reputable factory supply Difenoconazole 119446-68-3 in stock with high standard

  • Molecular Formula:C19H17Cl2N3O3
  • Molecular Weight:406.268
  • Appearance/Colour:colorless solid 
  • Vapor Pressure:5.09E-12mmHg at 25°C 
  • Melting Point:76 °C 
  • Refractive Index:1.641 
  • Boiling Point:547 °C at 760 mmHg 
  • PKA:2.94±0.12(Predicted) 
  • Flash Point:284.6 °C 
  • PSA:58.40000 
  • Density:1.41g/cm3 
  • LogP:4.66550 

Difenoconazole(Cas 119446-68-3) Usage

Definition

ChEBI: A member of the class of dioxolanes that is 1,3-dioxolane substituted at position 2 by 2-chloro-4-(4-chlorophenoxy)phenyl and 1,2,4-triazol-1-ylmethyl groups. A broad spectrum fungicide with novel broad-range activity used as a spray or seed treatment. It is moderately toxic to humans, mammals, birds and most aquatic organisms.

Agricultural Uses

Fungicide: For suppression of fungi diseases in crops and seeds.

Trade name

CGA 169374?; DIVIDEND?; DIVIDEND? EXTREME FUNGICIDE; HELIX?; SCORE?; TECHNICAL CGA-169374?

Metabolic pathway

There is limited published information on the metabolism of difenoconazole. It is slowly dissipated in soils, and metabolism in plants involves rupture of the triazole linkage or oxidation of the phenyl ring followed by conjugation.

Degradation

Difenoconazole is stable to hydrolysis and is thermally stable to 150 °C. DT50 of difenocoazole in natural sunlight was 145 days.

InChI:InChI=1/C19H17Cl2N3O3/c1-13-9-25-19(27-13,10-24-12-22-11-23-24)17-7-6-16(8-18(17)21)26-15-4-2-14(20)3-5-15/h2-8,11-13H,9-10H2,1H3

119446-68-3 Relevant articles

Triazole compound containing dioxolame and preparation method of intermediate of triazole compound

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Paragraph 0035; 0039, (2021/09/04)

The invention relates to a preparation m...

Method for synthesizing high-purity difenoconazole

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, (2021/02/10)

The invention discloses a method for syn...

Method for converting 4 - H difenoconazole isomer into 1 - H-difenoconazole (by machine translation)

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Paragraph 0033-0046, (2020/07/21)

A method for converting 4 - H-difenocona...

APPLICATION OF TETRAHYDROBENZAZOLE IN PREPARATION OF AGRICULTURAL FUNGICIDE OR FUNGICIDE COMPOSITION AND PREPARATION METHOD THEREOF

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Paragraph 0053-0055, (2020/04/10)

An application of tetrahydrobenzazole in...

119446-68-3 Process route

1,2,4-Triazole
288-88-0

1,2,4-Triazole

2-(bromomethyl)-2-(2-chloro-4-(4-chlorophenoxy)phenyl)-4-methyl-1,3-dioxolane
873012-43-2

2-(bromomethyl)-2-(2-chloro-4-(4-chlorophenoxy)phenyl)-4-methyl-1,3-dioxolane

difenconazole
119446-68-3

difenconazole

Conditions
Conditions Yield
With potassium carbonate; potassium iodide; In N,N-dimethyl-formamide; at 185 ℃; for 0.25h; Solvent; Temperature; Reagent/catalyst; Microwave irradiation;
92.6%
With trimethyldodecylammonium chloride; potassium hydroxide; In 1-methyl-pyrrolidin-2-one; at 130 ℃; Reagent/catalyst;
83%
With potassium carbonate; for 10h;
75.6%
With potassium carbonate; In 1-methyl-pyrrolidin-2-one; at 163 ℃; for 5.5h; Temperature;
27 g
C<sub>19</sub>H<sub>19</sub>Cl<sub>2</sub>N<sub>4</sub>O<sub>3</sub><sup>(1+)</sup>*Br<sup>(1-)</sup>

C19H19Cl2N4O3(1+)*Br(1-)

difenconazole
119446-68-3

difenconazole

Conditions
Conditions Yield
C19H19Cl2N4O3(1+)*Br(1-); With hydrogenchloride; sodium nitrite; In water; at 5 - 20 ℃; for 2h;
With water; at 40 ℃; Temperature; Alkaline conditions;
95%

119446-68-3 Upstream products

  • 288-88-0
    288-88-0

    1,2,4-Triazole

  • 873012-43-2
    873012-43-2

    2-(bromomethyl)-2-(2-chloro-4-(4-chlorophenoxy)phenyl)-4-methyl-1,3-dioxolane

  • 106-48-9
    106-48-9

    4-chloro-phenol

  • 2234-16-4
    2234-16-4

    1-(2,4-dichlorophenyl)ethan-1-one

119446-68-3 Downstream products

  • 186259-71-2
    186259-71-2

    2-{2-[2-chloro-4-(4-chlorophenoxy)-phenyl]-4-methyl-[1,3]dioxolan-2-ylmethyl}-2,4-dihydro[1,2,4]triazole-3-thione

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