151830-35-2

Usage

Uses

Used in Chemical Synthesis:
Methyl N-hydroxy-2-methylphenylcarbamate is used as an intermediate in the synthesis of Pyrametostrobin (P847010), a novel fungicide. Its role in the chemical synthesis process is crucial for the development of this new class of fungicides, which can help in controlling fungal infections in agriculture and other industries.
Used in Environmental Management:
Given its origin from 1-Methyl-2-nitrobenzene, a toxic environmental pollutant, methyl N-hydroxy-2-methylphenylcarbamate can be utilized in the development of methods to mitigate the environmental impact of this pollutant. By finding ways to convert or neutralize the pollutant through the synthesis of useful compounds like methyl N-hydroxy-2-methylphenylcarbamate, it can contribute to cleaner and more sustainable industrial processes.
Used in Pharmaceutical Research:
Methyl N-hydroxy-2-methylphenylcarbamate's carcinogenic activity in rats makes it a potential candidate for further research in the pharmaceutical industry. Understanding its mechanism of action and how it interacts with biological systems can provide valuable insights into the development of new drugs or the improvement of existing ones, particularly in the field of oncology.

Upstream product

• 88-72-2 1-methyl-2-nitrobenzene 
• 79-22-1 methyl chloroformate 
• 67-56-1 methanol 
• 201230-82-2 carbon monoxide 
• 611-22-3 N-(o-tolyl)hydroxylamine 
• 1157855-14-5 methyl N-2-tolyl-N-(methoxycarbonyloxy)carbamate 
• 65440-83-7 O-(2-methylphenyl)hydroxylamine 

Downstream Products

• 151827-83-7 methyl N-(2-bromomethylphenyl)-N-methoxy-carbamate 
• 1257424-08-0 methyl 2-((1-(4-chloro-2-fluoro-5-(methylsulfonamido)phenyl)-3-methyl-5-oxo-1H-1,2,4-triazol-4(5H)-yl)methyl)phenyl(methoxy)carbamate 
• 1257424-09-1 methyl 2-((1-(4-chloro-5-(ethylsulfonamido)-2-fluorophenyl)-3-methyl-5-oxo-1H-1,2,4-triazol-4(5H)-yl)methyl)phenyl(methoxy)carbamate 
• 1257424-10-4 methyl 2-((1-(4-chloro-2-fluoro-5-(phenylsulfonamido)phenyl)-3-methyl-5-oxo-1H-1,2,4-triazol-4(5H)-yl)methyl)phenyl(methoxy)carbamate 
• 1257424-11-5 methyl 2-((1-(2,4-dichloro-5-(methylsulfonamido)phenyl)-3-methyl-5-oxo-1H-1,2,4-triazol-4(5H)-yl)methyl)phenyl(methoxy)carbamate 
• 1257424-12-6 methyl 2-((1-(2,4-dichloro-5-(ethylsulfonamido)phenyl)-3-methyl-5-oxo-1H-1,2,4-triazol-4(5H)-yl)methyl)phenyl(methoxy)carbamate 
• 1257424-13-7 methyl 2-((1-(2,4-dichloro-5-(phenylsulfonamido)phenyl)-3-methyl-5-oxo-1H-1,2,4-triazol-4(5H)-yl)methyl)phenyl(methoxy)carbamate 
• 151827-82-6 methyl N-(2-methylphenyl)-N-methoxy-carbamate 
• 175013-18-0 pyraclostrobin 
• 1218786-69-6 N-methoxycarbonyl-2-(2',2',2'-trichloroacetylamino)-6-methylaniline 

Relevant academic research and scientific papers

Bactericidal composition containing isotianil and osthole

The invention discloses a bactericidal composition containing isotianil and osthole, and belongs to the technical field of pesticide preparation. The bactericidal composition comprises, by weight, 1-50% of isotianil, 0.1-10% of osthole, 5-10% of a bacteri

PRODUCTION OF N-SUBSTITUTED AROMATIC HYDROXYLAMINE

An economic, one-step method for the production of N-substituted aromatic hydroxylamines of formula (I) [in-line-formulae]R—N(OH)—C(═O)—(O)R1??(I),[/in-line-formulae] with hydrogen, by catalytic hydration with possibly modified hydration catalysts in an aprotic solvent and in the presence of a halogen formic acid ester and in some cases in the presence of a base.

Synthetic method of N-methoxy-N-2-methylphenylcarbamate

The invention provides a synthetic method of N-methoxy-N-2-methylphenylcarbamate. The synthetic method comprises the following main steps: firstly, adding ortho-nitrotoluene and an aqueous solution of NH4Cl into metal zinc, dimethyl sulfoxide and methanol

Synthesis technology of pyraclostrobin

The invention provides a synthesis technology of pyraclostrobin. The method comprises the following steps that1, ortho-nitrotoluene and NH4Cl are subjected to a reduction reaction under the catalytic action of zinc powder and alloy micro-nano powder; 2, hydroxylamine is subjected to an acylation reaction; 3, a methylation reaction is performed; 4, a bromination reaction is performed to obtain N-methoxy-N-2-methyl bromide methyl phenyl carbamate; 5, DMF is used as a solvent for dissolving the N-methoxy-N-2-methyl bromide methyl phenyl carbamate to prepare a solution for use, 1-(4-chlorphenyl)-pyrazol alcohol, K2CO3 and acetone are placed into a reactor together, heating and reflux are performed, the N-methoxy-N-2-methyl bromide methyl phenyl carbamate solution is added into the reactor slowly, and after the reflux reaction is ended, pyraclostrobin is obtained. Compared with the prior art, the preparation method is simple, raw materials are low in cost and easy to obtain, the reaction conditions are mild, and the obtained target product is high in purity and yield.

Synthesis and biological activity of novel phenyltriazolinone derivatives

Phenyltriazolinones are one of the most important classes of herbicides targeting the protoporphyrinogen oxidase enzyme. A series of triazolinone derivatives containing a strobilurin pharmacophore were designed and synthesized with the aim of discovering new phenyltriazolinone analogues with high activity. The herbicidal activity of the synthesized compounds was assayed and some of the test compounds displayed moderate herbicidal activity at 150 g ai/ha.

Facile procedure for the synthesis of N-aryl-N-hydroxy carbamates

An efficient one-pot procedure for the zinc-mediated reduction of nitroarenes in the presence of chloroformates leading to the corresponding N,O-bisprotected hydroxylamine is described. Reactions proceed smoothly under ambient conditions in THF-water mixt

Dihydropyridazinones and pyridazinones and their use as fungicides and insecticides

Compounds with fungicidal and insecticidal properties having formula I wherein W is n is 0 or 1; Y is O, S, NR1, or R6; the ring bond containing R4 and R5 is a single or double bond; X is independently selected from hydrogen, halo, (C1-C4)alkyl, (C1-C4)al

Carbamates and crop protection agents containing them

Carbamates of the formula I STR1 where the substituents have the following meanings: Z is methoxy, NH2, NHCH3, N(CH3)2, CH3, C2 H5, CF3 or CCl3, X and Y are

Dihydropyridazinones and pyridazinones and their use as fungicides and insecticides

Compounds with fungicidal and insecticidal properties having formula I wherein W is n is 0 or 1; Y is O, S, NR1, or R6; the ring bond containing R4and R5is a single or double bond; X is independently selected fr