2655-14-3 Usage
Description
3,5-Xylyl methylcarbamate, also known as XMC, is an organic compound that serves as an effective insecticide. It is characterized by its contact action, which means it works by making direct contact with the target pests, leading to their paralysis and eventual death.
Uses
Used in Agriculture:
3,5-Xylyl methylcarbamate is used as an insecticide for the control of various pests, particularly leafhoppers and planthoppers, which are known to cause significant damage to rice crops. Its application helps protect the rice plants from these pests, ensuring a healthy yield.
Used in Tea Crop Protection:
In addition to its use in rice crops, 3,5-Xylyl methylcarbamate is also employed as a pesticide in the protection of green tea crops. It is specifically used to control tea green leafhoppers, which can cause severe damage to tea plants if left unchecked. By using XMC, tea farmers can maintain the quality and quantity of their tea harvest.
Used in Pesticide Formulation:
3,5-Xylyl methylcarbamate is an essential component in the formulation of various pesticides. Its inclusion in these formulations enhances their effectiveness against a range of pests, making it a valuable asset in the agricultural industry.
Metabolic pathway
Metabolic pathways for XMC involve hydroxylation of ring-methyl
groups, N-methyl groups and of the phenyl ring. Hydrolysis of the ester
moiety occurs in soils.
Degradation
XMC is rapidly hydrolysed in alkaline media to afford the phenol (2). It is
relatively stable in neutral and weakly acidic aqueous solutions even at
temperatures up to 90 °C. Aqueous solutions of XMC are stable to light(PM).
Check Digit Verification of cas no
The CAS Registry Mumber 2655-14-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,5 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2655-14:
(6*2)+(5*6)+(4*5)+(3*5)+(2*1)+(1*4)=83
83 % 10 = 3
So 2655-14-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO2/c1-7-4-8(2)6-9(5-7)13-10(12)11-3/h4-6H,1-3H3,(H,11,12)
2655-14-3Relevant articles and documents
An easy and efficient one-step procedure for the preparation of alkyl and aryl alkylcarbamates from S-methyl N-alkylthiocarbamates
Degani, Iacopo,Fochi, Rita,Magistris, Claudio
experimental part, p. 2919 - 2924 (2009/04/06)
A general, one-step procedure for the synthesis of alkyl and aryl alkylcarbamates, by the direct reaction of S-methyl N-alkylthiocarbamates with alcohols or phenols in toluene at reflux in the presence of triethylamine, is reported. All the target products were obtained in high yield (15 examples, average yield 94%) and very high purity (>99.2%). The recovery of a co-product of industrial interest, methanethiol, in an amount of one mole for each mole of thiocarbamate, with complete exploitation of the reagent, should also be noted. Georg Thieme Verlag Stuttgart.
Fluid insecticidal formulations for treatment of parasitic insect larvae by dermal application
-
, (2008/06/13)
The present invention relates to the use of polysiloxanes containing at least one quaternary ammonium group as formulation auxiliary in formulations of larvicidal and/or ovicidal active compounds and to compositions containing a) a larvicidal and/or ovicidal active compound and b) a polysiloxane derivative with at least one quaternary ammonium group per molecule, and, if appropriate, further auxiliaries and carriers.
Pyrazole oxime derivatives and compositions
-
, (2008/06/13)
A pyrazole oxime derivative represented by the general formula (I) which is useful as an insecticide and fungicide, STR1 wherein the structural elements are defined in the specification, and the method of controlling said pests. The compounds represented by the general formula (I) can be synthesized by the methods disclosed in the specification.
