22259-30-9 Usage
Description
Formetanate, also known as 3-dimethylaminomethyleneaminophenyl methylcarbamate (IUPAC), is a pesticide with yellow crystalline structure and low solubility in water (<1 g/L at 20°C). It is soluble in acetone, chloroform, and methanol. Formetanate is synthesized by reacting 3-dimethylaminomethyleneaminophenol with methyl isothiocyanate and is known for its activity against the mobile stages of fruit tree spider mites.
Uses
Used in Agriculture:
Formetanate is used as an acaricide for deciduous fruits, specifically targeting and controlling the mobile stages of fruit tree spider mites, which can cause significant damage to the crops.
Used in Pesticide Residue Management:
Formetanate is also used as a pesticide residue in table grapes, green peppers, and cucumbers. It serves as a multi-application pesticide, providing protection against various pests and ensuring the quality and safety of these produce items.
Used in Chemical Industry:
Due to its water solubility and chemical properties, formetanate can be utilized in the chemical industry for various purposes, such as in the formulation of pesticides or as an intermediate in the synthesis of other compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 22259-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,5 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22259-30:
(7*2)+(6*2)+(5*2)+(4*5)+(3*9)+(2*3)+(1*0)=89
89 % 10 = 9
So 22259-30-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H15N3O2/c1-12-11(15)16-10-6-4-5-9(7-10)13-8-14(2)3/h4-8H,1-3H3,(H,12,15)/b13-8-
22259-30-9Relevant articles and documents
HYDROLYSIS KINETICS AND MECHANISM OF N'-(3-N-METHYLCARBAMOYLOXYPHENYL)-N,N-DIMETHYLFORMAMIDINE
Cegan, Alexandr,Slosar, Jaroslav,Vecera, Miroslav
, p. 1065 - 1071 (2007/10/02)
Hydrolysis of N'-(3-N-methylcarbamoyloxyphenyl)-N,N-dimethylformamidine (I) has been studied in mixture water-dioxane (4:1) at pH 1 to 13.The hydrolysis rates of methylcarbamoyl and dimethylformamidine groups are comparable within pH range 4 to 10, and they differ by as much as several orders of magnitude in pH ranges 1-3 and 11-13.The hydrolysis products of the whole pH range have been determined by paper chromatography, and reaction mechanism has been suggested on the basis of the measured hydrolysis rate constants.Effects of protonation and hydratation of dimethylformamidine group on the hydrolysis rate of the methylcarbamoyl group is discussed.