99387-89-0 Usage
Description
Triflumizole is a broad-spectrum fungicide that is effective in controlling various fungal pathogens in agricultural crops. It is a member of the phenylpyrrole class of fungicides and works by inhibiting the enzyme demethylase, which is essential for the synthesis of ergosterol, a vital component of fungal cell membranes. This disruption leads to the weakening and eventual death of the fungal cells.
Uses
Used in Pome Fruit Industry:
Triflumizole is used as a fungicide for the control of Gymnospurangum and Venturia spp. in pome fruit. It helps protect the fruit from infections and diseases caused by these fungal pathogens, ensuring a healthy and high-quality harvest.
Used in Vegetable Industry:
In the vegetable industry, Triflumizole is used as a protective agent against powdery Erysiphaceae, a group of fungi that cause powdery mildew on various vegetable crops. This helps maintain the quality and yield of the vegetables, reducing crop losses due to fungal infections.
Used in Cereal Industry:
Triflumizole is used as a seed treatment in the cereal industry to protect against Helminthosporium, Tilletia, and Ustilago spp. These fungi can cause significant damage to cereal crops, and the use of Triflumizole helps to minimize the impact of these pathogens on crop yields and quality.
Used in General Agriculture:
Triflumizole is also used in general agriculture for the control of Fusarium, Fulvia, and Monilia spp. These fungi can cause various diseases in a wide range of crops, and the application of Triflumizole helps to protect plants from these infections, ensuring a healthy and productive agricultural output.
Metabolic pathway
Triflumizole is unstable in aqueous solution when exposed to light and
it is readily metabolised by plants and animals. The primary route
of metabolism is by cleavage of the imidazole ring to give several
metabolites which retain the 4-chloro-2-trifluoromethylaniline moiety.
The major metabolite in crops, 2, is formed by loss of the imidazole
ring.
Degradation
Aqueous solutions of triflumizole are degraded by sunlight with a DT50 of
29 hours. The sole hydrolysis product of triflumizole in the dark is 2,
which is formed by loss of the imidazole ring.
The major product of photolysis of triflumizole is 4, which is probably
formed in the presence of oxygen via 3. This compound was soluble in the
solid state but decomposed in solution, even if stored in a refrigerator
(Hashimoto et al., 1990).
Check Digit Verification of cas no
The CAS Registry Mumber 99387-89-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,8 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 99387-89:
(7*9)+(6*9)+(5*3)+(4*8)+(3*7)+(2*8)+(1*9)=210
210 % 10 = 0
So 99387-89-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H15ClF3N3O/c1-2-7-23-9-14(22-6-5-20-10-22)21-13-4-3-11(16)8-12(13)15(17,18)19/h3-6,8,10H,2,7,9H2,1H3
99387-89-0Relevant articles and documents
Pyrazolyl benzyl ether derivatives containing a fluoromethoxyimino group and use thereof as pesticides
-
, (2008/06/13)
The invention relates to novel pyrazolyl benzyl ethers, to a plurality of processes for their preparation and to their use for controlling harmful organisms.
Patch preparations for treating plants
-
, (2008/06/13)
The following invention introduces a patch preparation for treating plants, whereas the patch preparations comprise a chemical layer composed of at least one agrochemically active compound, at least one adhesive and optionally, one or more additives. The components are dispersed in a matrix state on a substrate which are then introduced on the roots of the plant to be treated.
Microbicidal benzotriazoles
-
, (2008/06/13)
Novel benzotriazoles of the formula STR1 in which R, X1, X2, X3, X4 and Y have the meanings given in the description, and their acid addition salts and metal salt complexes, a process for the preparation of these substances and their use as microbicides in crop protection and in material protection.
