953075-90-6

Usage

Uses

Used in Organic Synthesis:
2,6-diethyl-4-methylphenyl boronic acid serves as a crucial reagent in Suzuki-Miyaura cross-coupling reactions, which are pivotal for the formation of carbon-carbon bonds. Its ability to engage in stable complex formation with diols makes it an indispensable component in this widely utilized method.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 2,6-diethyl-4-methylphenyl boronic acid emerges as a potential scaffold for the development of novel drugs. Its unique structural features allow it to target specific biological markers, offering a promising avenue for creating effective therapeutic agents.
Used in Material Science:
Beyond its applications in synthesis and medicine, 2,6-diethyl-4-methylphenyl boronic acid also finds relevance in material science. Its properties contribute to the advancement of material development, where its interaction with other compounds can lead to innovative material compositions.

Upstream product

• 314084-61-2 1-bromo-2,6-diethyl-4-methylbenzene 
• 121-43-7 Trimethyl borate 

Downstream Products

• 1415576-44-1 C₂₅H₂₅F₅O₂S 
• 1415576-05-4 C₂₆H₂₉F₃O₃S 
• 1415576-48-5 C₂₄H₂₈N₂O₄S 
• 1415576-49-6 C₂₇H₃₂F₃NO₂S 
• 1415575-95-9 C₂₈H₃₃F₃O₂S 
• 1415575-96-0 C₂₇H₃₂F₃NO₂S 
• 1415575-97-1 C₂₈H₃₁F₃O₂S 
• 1415578-15-2 C₂₆H₃₂O₃ 
• 1415578-16-3 C₂₈H₃₄O₄ 
• 1415578-17-4 C₂₁H₂₈O₄ 
• 1415575-75-5 C₂₆H₂₉F₃O₂S 
• 1415576-07-6 C₂₄H₂₉NO₂S 
• 1415576-51-0 C₂₅H₃₁NO₂S 
• 1415576-52-1 C₃₄H₃₇NO₄S 

Relevant academic research and scientific papers

Method for synthesizing 2,6-diethyl-4-methylphenylacetate

The invention relates to the technical field of organic synthesis, in particular to a method for synthesizing 2,6-diethyl-4-methylphenylacetate by taking 2,6-diethyl-4-methylbromobenzene as a raw material, which comprises the following steps: firstly reacting 2,6-diethyl-4-methylbromobenzene with n-butyllithium and then conducting reacting with borane trimethyl ester to generate 2,6-diethyl-4-methylphenylboronic acid; and reacting the 2,6-diethyl-4-methylphenylboronic acid with glycine alkyl ester hydrochloride to generate the 2,6-diethyl-4-methylphenylacetate. The preparation method of the 2,6-diethyl-4-methyl phenylacetate provided by the invention has the advantages that the steps are fewer, the use of an expensive noble metal catalyst and a highly toxic cyaniding reagent is avoided, the cost is reduced, the process is simplified, the yield is higher, the defects in the prior art are overcome, and the preparation method is suitable for large-scale industrial production.

USE OF PYRIDAZINONE COMPOUND FOR CONTROL OF HARMFUL ARTHROPOD PESTS

Since a pyridazinone compound shown by formula (I) has an activity for controlling arthropod pests, the pyridazinone compound is effective for a use for controlling arthropod pests.

HERBICIDAL COMPOSITION

There is provided a herbicidal composition containing compound represented by the formula (I) : a compound represented by the formula (I) : wherein R1 represents a C1 - 6 alkyl group etc., R2 represents hydrogen etc., G re

HERBICIDAL COMPOSITION

A herbicidal composition having an excellent weed control effect, which comprises a pyridazinone compound represented by the formula (I): wherein R1 represents a C1-6 alkyl group or a (C1-6 alkyloxy) C1-6 alkyl

HERBICIDAL COMPOSITION

A herbicidal composition having an excellent weed control effect, which comprises a pyridazinone compound represented by the formula (I) : wherein R1 represents a C1-6 alkyl group or a (C1-6 alkyloxy) C1-6 alkyl

HERBICIDAL COMPOSITION

A herbicidal composition having an excellent weed control effect, which comprises a pyridazinone compound represented by the formula (I): wherein R1 represents a C1-6 alkyl group or a (C1-6 alkyloxy) C1-6 alkyl

NOVEL HERBICIDES

Cyclohexanedione compounds, and derivatives thereof, which are substituted in 5-position, are suitable for use as herbicides.

2-ARYL-5-HETEROCYCLYL-CYCLOHEXANE-1,3-DIONE COMPOUNDS AND THEIR USE AS HERBICIDES

Cyclohexanedione compounds of Formula (I) wherein R1 is methyl, ethyl, n-propyl, iso-propyl, cyclopropyl, halomethyl, haloethyl, halogen, vinyl, ethynyl, methoxy, ethoxy, halomethoxy or haloethoxy, R2 and R3 are, independently hydrogen, halogen, C1-C6alkyl, C1-C6haloalkyl, C1-C6alkoxy, C1-C6haloalkoxy, C2-C6alkenyl, C2-C6haloalkenyl, C2-C6alkynyl, C3-C6alkenyloxy, C3-C6haloalkenyloxy, C3-C6alkynyloxy, C3-C6cycloalkyl, C1-C6alkylthio, C1-C6alkylsulfinyl, C1-C6alkylsulfonyl, C1-C6alkylsulfonyloxy, C1-C6haloalkylsulfonyloxy, cyano, nitro, phenyl, phenyl substituted by C1-C4alkyl, C1-C3Cahaloalkyl, C1-C3alkoxy, C1-C3haloalkoxy, cyano, nitro, halogen, C1-C3alkylthio, C1-C3alkylsulfιnyl or C1-C3alkylsulfonyl, or heteroaryl or heteroaryl substituted by C1-C3Calkyl, d.Cahaloalkyl, C1-C3aIkoxy, C1-C3haloalkoxy, cyano, nitro, halogen, C1-C3alkylthio, C1-C3alkylsulfinyl or C1-C3alkylsulfonyl, R4 is hydrogen, methyl, ethyl, n-propyl, iso-propyl, halomethyl, haloethyl, halogen, vinyl, ethynyl, methoxy, ethoxy, halomethoxy or haloethoxy, X is O, S, S(O) or S(O)2, R5 is hydrogen or methyl, R6 is hydrogen, methyl or ethyl, or forms a double bond, which links the carbon atom, to which R6is attached, with the adjacent carbon atom of R7 or R8, R7 and R8 are independently of each other C1-C5alkylene, which is unsubstituted or substituted by methyl or ethyl, or C2-C5alkenylene, which is unsubstituted or substituted by methyl or ethyl, and G is hydrogen, an alkali metal, alkaline earth metal, sulfoniυm, ammonium or a latentiating group, are suitable for use as herbicides.

PYRIDAZINONE COMPOUND AND USE THEREOF AS HERBICIDES

A pyridazinone compound represented by the formula (I) have excellent effect on weed control and are useful as an active ingredient of herbicides.