71626-11-4 Usage
Description
Benalaxyl is an acylamino acid fungicide that is widely used in the agricultural industry for the control of Oomycetes on a variety of crops, fruits, flowers, ornamentals, and turf. It is known for its effectiveness in protecting plants from various fungal diseases, ensuring a healthy and productive yield.
Uses
Used in Agricultural Industry:
Benalaxyl is used as a fungicide for the control of Oomycetes on a wide range of crops, fruits, flowers, ornamentals, and turf. It helps in preventing and treating various fungal diseases, ensuring the health and productivity of the plants.
Used in Crop Protection:
Benalaxyl is used as a crop protection agent, providing a shield against Oomycetes that can cause significant damage to the plants. By controlling these pathogens, it helps in maintaining the quality and quantity of the agricultural produce.
Used in Fruit and Vegetable Production:
In the fruit and vegetable production industry, Benalaxyl is used as a fungicide to protect the plants from fungal infections. This ensures that the fruits and vegetables remain healthy and free from diseases, leading to better quality produce and higher yields.
Used in Ornamental and Turf Management:
Benalaxyl is also used in the ornamental and turf management industries to control Oomycetes and other fungal pathogens. This helps in maintaining the aesthetic appeal and health of the ornamental plants and turf, making them more resistant to diseases and environmental stressors.
Metabolic pathway
The fate of 14C-benalaxyl as affected by mancozeb is
determined on the surface and in the tissues of grape
leaves 7 days after the single foliar application of a
mixture with mancozeb. The main oxidative scheme
with rat liver microsomes is quite similar to that
observed in plants. The only differences are
represented by a further hydroxylation on the second
ortho methyl group, and only traces of the meta
hydroxylation take place on the xylene ring.
Degradation
Benalaxyl is stable in aqueous media over a wide pH range but it is hydrolysed
in concentrated alkali. Its DT50 at pH 9 and 25 °C is 86 days (PM).
It is reasonably stable to sunlight in aqueous solution. When irradiated
in solution with UV light (254 nm) it is degraded with a half-life of
55 minutes (Pirisi et al., 1996). Products were compounds 2 and 3 (see
Scheme 1) which are common also to metalaxyl and furalaxyl. These
were detected in a non-labelled study. Under simulated sunlight its
half-life was 167 days.
Check Digit Verification of cas no
The CAS Registry Mumber 71626-11-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,2 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71626-11:
(7*7)+(6*1)+(5*6)+(4*2)+(3*6)+(2*1)+(1*1)=114
114 % 10 = 4
So 71626-11-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H23NO3/c1-14-9-8-10-15(2)19(14)21(16(3)20(23)24-4)18(22)13-17-11-6-5-7-12-17/h5-12,16H,13H2,1-4H3/t16-/m0/s1
71626-11-4Relevant articles and documents
SUBSTITUTED SPIROCYCLIC KETOENOLS
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, (2008/06/13)
The present invention relates to novel substituted spirocyclic ketoenols of the formula (I) in which W, X, Y, Z, A, B, D and G are as defined in the disclosure, to a plurality of processes for their preparation and to their use as pesticides, microbicides and herbicides.
Use of oxabicyclo[2.2.1]heptane derivatives as pesticidal agents
-
, (2008/06/13)
7-oxabicyclo[2.2.1]heptane derivatives of formula (I) in which X, R1, R2, R3 and R4 have the meanings set forth in the specification, are very suitable for controlling undesired microorganisms and animal pests. New 7-oxabicyclo[2.2.1]heptane derivatives of formula (Ia) in which X, R1, R2, R3 and R14 have the meanings set forth in the specification, and a process for the preparation of the new compounds.
Heterocyclic fluoroalkenyl thioethers and the use thereof as pesticides(III)
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, (2008/06/13)
The present invention relates to novel heterocyclic fluoroalkenyl thioethers of the formula (I) in which X represents hydrogen, halogen or alkyl, m represents integers from 3 to 10, n represents 0, 1 or 2, Y represents sulphur or oxygen, R1 represents halogen, represents in each case optionally halogen-substituted alkyl, alkoxy, alkylthio, alkenyl, alkenyloxy, alkenylthio or alkylcarbonyl, represents optionally substituted cycloalkyl, represents optionally substituted aryl or represents optionally substituted heterocyclyl and R2 represents hydrogen, halogen, represents in each case optionally halogen-substituted alkyl, alkoxy, alkylthio, alkenyl, alkenyloxy, alkenylthio or alkylcarbonyl, represents optionally substituted cycloalkyl, represents optionally substituted aryl or represents optionally substituted heterocyclyl, ?except for compounds where R1=alkyl, Y=oxygen and X=hydrogen, and to processes for their preparation and to their use as pesticides.