79533-04-3

Usage

Uses

Used in Agricultural Industry:
Methiocarb is used as an insecticide and acaricide for controlling pests on crops and ornamental plants, ensuring the protection and health of plants, and contributing to increased agricultural productivity.
Used in Public Health Applications:
In public health, methiocarb is utilized to control pests that can transmit diseases or cause discomfort, thereby improving the overall well-being and safety of communities.
Despite its effectiveness, the use of methiocarb is restricted in some areas due to concerns about its potential impact on non-target organisms and the environment. It is essential to follow proper safety precautions and regulations when handling and applying (4-ACETYL-PHENYL)-METHYL-CARBAMIC ACID TERT-BUTYL ESTER to minimize any adverse effects.

Upstream product

• 56-91-7 p-aminomethylbenzoic acid 
• 314732-37-1 tert-butyl 4-(methoxy(methyl)carbamoyl)benzylcarbamate 
• 75-16-1 methylmagnesium bromide 
• 33233-67-9 4-(tert-Butoxycarbonylaminomethyl)benzoic acid 
• 1314538-55-0 potassium tert-butyl N-[(trifluorolambda-4-boranyl)methyl]carbamate 
• 69497-83-2 4-acetylphenyl mesylate 
• 1432739-32-6 4-acetylphenyl N,N-dimethylsulfamate 
• 99-93-4 4-Hydroxyacetophenone 
• 99-91-2 para-chloroacetophenone 
• 79533-03-2 N-BOC-p-aminomethylacetophenone ethylene ketal 

Downstream Products

• 79533-05-4 [4-(tert-butoxycarbonylamino-methyl)-phenyl]-oxo-acetic acid 
• 1202804-50-9 1-(4-(aminomethyl)phenyl)ethanone trifluoroacetate salt 

Relevant academic research and scientific papers

Pd-catalyzed Suzuki-Miyaura cross-coupling reactions between sulfamates and potassium Boc-protected aminomethyltrifluoroborates

Sulfamates were studied as the electrophilic partners in the palladium-catalyzed Suzuki-Miyaura cross-coupling reaction with potassium Boc-protected primary and secondary aminomethyltrifluoroborates. A broad range of substrates was successfully coupled to provide the desired products. Complex molecules containing a new carbon-carbon bond and an aminomethyl moiety could be prepared through this developed method.

Suzuki-Miyaura cross-coupling reactions of potassium boc-protected aminomethyltrifluoroborate with aryl and hetaryl mesylates

Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions were studied with potassium Boc-protected aminomethyltrifluoroborate through C-O activation of various mesylate derivatives to afford the corresponding products in moderate to good yields.

Targeting the von Hippel-Lindau E3 ubiquitin ligase using small molecules to disrupt the VHL/HIF-1α interaction

E3 ubiquitin ligases, which bind protein targets, leading to their ubiquitination and subsequent degradation, are attractive drug targets due to their exquisite substrate specificity. However, the development of small-molecule inhibitors has proven extrao

Synthesis and Suzuki-Miyaura cross-coupling reactions of potassium Boc-protected aminomethyltrifluoroborate with aryl and hetaryl halides

Potassium Boc-protected aminomethyltrifluoroborate, a primary aminomethyl equivalent, was synthesized successfully through a "one-pot" process. With this trifluoroborate, Suzuki-Miyaura cross-coupling reactions were investigated with a variety of both aryl and hetaryl chlorides in good to excellent yields.

Cephem compounds having a terminal aminocarboxylic acid grouping and containing an azacyclyl(thio)ureido group

Compounds of the formula STR1 in which the index n represents an integer of from 1 to 4, the index m represents 0 or 1, X represents oxygen, sulphur or the group --NH--, W represents a group --CO--, --CO--NHSO2 -- or --SO2 NH--CO--, or X-W together represent a group --CO-- or --CO--NHSO2 --, A represents optionally substituted phenylene, thienylene or furylene, Z represents oxygen or sulphur, Y represents lower alkylene, the index k represents the value 1 or 2, R4 represents hydrogen, an optionally substituted lower aliphatic or cycloaliphatic radical or acyl, R1 represents hydrogen, lower alkyl, lower alkoxy, halogen or a group of the formula --CH2 --R2 in which R2 represents a free, esterified or etherified hydroxy or mercapto group or a quaternary ammonium group, and R3 represents hydrogen or methoxy, and in which the carboxyl groups are optionally esterified in a form that can be split under physiological conditions, and salts of such compounds having salt-forming groups, are obtained by liberating the functional group(s) in a compound of the formula I in which at least one of the functional groups present is protected. The compounds are effective in vitro and in vivo against gram-positive and gram-negative bacteria and cocci.