115199-26-3

Usage

Uses

Used in Pharmaceutical Industry:
(E)-Methyl-2-(2-bromomethylphenyl)-2-methoxyiminoacetate is used as an intermediate in the synthesis of pharmaceuticals for its antibacterial and antifungal properties. It contributes to the development of drugs that can effectively combat various infections and improve patient outcomes.
Used in Crop Protection Industry:
In the crop protection industry, (E)-Methyl-2-(2-bromomethylphenyl)-2-methoxyiminoacetate is used as an active ingredient in the formulation of pesticides and fungicides. Its antibacterial and antifungal properties help protect crops from diseases and pests, ensuring higher yields and better quality produce.
Used in Chemical Synthesis:
(E)-Methyl-2-(2-bromomethylphenyl)-2-methoxyiminoacetate is also used as a versatile building block in the synthesis of various organic compounds. Its unique structure allows for further functionalization and modification, enabling the creation of new molecules with potential applications in different fields.

Upstream product

• 115199-21-8 methyl 2-methyl-α-methoxyiminophenylacetate 
• 126534-57-4 methyl 2-(2'-bromomethylphenyl)-2-oxoacetate 
• 593-56-6 N-methoxylamine hydrochloride 

Relevant academic research and scientific papers

Synthesis, Antiviral Activity, and Induction of Plant Resistance of Indole Analogues Bearing Dithioacetal Moiety

A series of compounds with potential activity to induce plant resistance was synthesized from indole and thiol compounds and methodically evaluated for antiviral activity. The results indicated that some of the synthesized compounds had high antipotato virus Y (PVY), anticucumber mosaic virus, and antitobacco mosaic virus activities. Notably, compound D21 exhibited the best activity against PVY among these compounds in vivo, and the 50% effective concentrations (EC50) of protection activity is 122 μg/mL, which was distinctively better than the corresponding values for ribavirin (653 μg/mL), Ningnanmycin (464 μg/mL), and Xiangcaoliusuobingmi (279 μg/mL). Interestingly, we found that the protection activity of D21 was associated with improvement of chlorophyll content and defense-related enzyme activities. Moreover, D21 could trigger the malate dehydrogenase (MDH) signaling pathway, as further confirmed by the MDH activity evaluation. Hence, D21 can protect plants against viral activity and has potential as a novel activator for plant resistance induction.

A 2 - bromo methyl of compounds of preparation method

The invention discloses a method for preparing a 2-benzyl bromide compound. The method comprises the following steps: carrying out a contact reaction on a compound shown as a formula (2), an organic solvent and bromate in the presence of hydrosulphite and a catalyst, thereby obtaining a compound shown as a formula (1), wherein the structural formula is as shown in the description, and in the formula (1) and the formula (2), R1 refers to C1-C4 alkyl, R2 refers to C1-C4 alkyl, X refers to nitrogen atoms or oxygen atoms, and Z refers to CH or nitrogen atoms. According to the method for preparing the 2-benzyl bromide compound disclosed by the invention, the operation conditions are simple, the bromine utilization rate is high, corrosive gases are avoided, harm to the environment is avoided, the target product is high in selectivity and high in yield, and the method is mild in production conditions and low in production cost. Therefore, the method can be suitable for large-scale industrial production.

Oxime ether compound, processes for preparing the same and fungicide containing the same

Disclosed are an oxime ether compound represented by the formula (I): STR1 wherein R1 represents an alkyl group having 1 to 6 carbon atoms; R2 represents OR5 or NHR6 where R5 and R6 each represent an alkyl group having 1 to 6 carbon atoms; R3 represents a cycloalkyl group having 3 to 8 carbon atoms; R4 represents an alkenyloxy group having 3 to 6 carbon atoms, an alkynyloxy group having 3 to 6 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, a benzyloxy group, an alkoxycarbonyl group having 2 to 7 carbon atoms, a halogen atom, a cyano group, an alkylthio group having 1 to 6 carbon atoms, an alkyl group having 1 to 6 carbon atoms, a haloalkyl group having 1 to 6 carbon atoms or an acyl group having 2 to 7 carbon atoms; and n represents an integer of 0 to 5. processes for preparing the same and a fungicide containing the same as an effective ingredient.

Oxime ether derivatives, their preparation and fungicides containing these derivatives

Oxime ether derivatives of the formula I STR1 where R1 and R2 are each hydrogen or alkyl, Het is pyridyl, quinolyl, pyrimidinyl, pyrazinyl, pyridazinyl, thienyl, quinoxalinyl, isoxazolyl, benzoxazolyl or benzothiazolyl, the heterocyc

Aniline derivatives and fungicides containing them

Aniline derivatives of the formula STR1 where R is hydrogen, halogen, cyano, nitro, alkyl, cycloalkyl, alkenyl, alkoxy, haloalkyl, haloalkoxy, or substituted or unsubstituted phenyl, phenoxy, benzyl or benzyloxy, m is an integer from 1 to 5 or the group S

Sulfur-containing oxime ethers and fungicides containing them

Oxime ether derivatives of the formula STR1 where R1 and R2 are each hydrogen or alkyl, X is S, SO or SO2, R3 is hydrogen, cycloalkyl, phenyl, naphthyl, quinolinyl or phenanthrenyl, these radicals being unsubstituted or substituted, Y is alkylene, alkenylene or alkynylene, and m is 0 or 1.

Pest control with pyrimidines

Methods of combating pests with substituted pyrimidines of the formula I STR1 where R1 is alkyl, cycloalyl, haloalkyl, alkoxy, alkylthio or substituted or unsubstituted aryl, R2 is halogen or hydrogen, A is oxygen, or sulfur, and X i

Oxime ethers, their preparation and fungicides containing these compounds

Oxime ethers of the general formula STR1 where R1 and R2 are hydrogen or alkyl, R3 is hydrogen, halogen, cyano, aryl or aryloxy, the aromatic ring being unsubstituted or substituted, or R3 is heteroaryl, adamantyl, fluorenyl or cycloalkyl or cycloalkenyl, these radicals being unsubstituted or substituted, X is saturated or unsaturated C1 -C12 -alkylene which is unsubstituted or substituted, and n is 0 or 1, and fungicides containing these compounds.

Substituted N-hydroxypyrazoles and fungicides which contain these compounds

Substituted N-hydroxypyrazoles of the general formula STR1 where R1, R2 and R3 are identical or different and are hydrogen, alkyl, haloalkyl, cycloalkyl, alkoxycarbonyl, halogen, aryl or arylalkyl, the aromatic ring being