478685-71-1

Usage

Uses

Used in Organic Synthesis:
2-(Methoxymethoxy)-5-methylphenylboronic acid is used as a building block in organic synthesis for creating pharmaceuticals and other bioactive compounds. Its ability to form reversible covalent bonds with diols makes it a valuable reagent in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-(Methoxymethoxy)-5-methylphenylboronic acid is used as a versatile reagent for designing and developing new pharmaceuticals. Its unique structure allows for the creation of diverse molecular structures that can target specific biological processes and pathways, potentially leading to the discovery of novel therapeutic agents.
Used in Bioactive Compound Development:
2-(Methoxymethoxy)-5-methylphenylboronic acid is also used in the development of bioactive compounds, which are molecules that can interact with biological systems to produce a desired effect. 2-(Methoxymethoxy)-5-methylphenylboronic acid's ability to form reversible covalent bonds with diols makes it a promising candidate for the creation of bioactive molecules with potential applications in various industries, such as pharmaceuticals, agriculture, and materials science.

Upstream product

• 104750-60-9 2-bromo-1-(methoxymethoxy)-4-methylbenzene 
• 5419-55-6 Triisopropyl borate 
• 25458-49-5 1-(methoxymethoxy)-4-methylbenzene 
• 121-43-7 Trimethyl borate 
• 6627-55-0 2-bromo-p-cresol 

Downstream Products

• 854779-53-6 6-{[[1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazol-4-ylmethyl]-(1-methyl-1H-imidazol-2-ylmethyl)-amino]-methyl}-nicotinic acid methyl ester 
• 675583-74-1 6-{[[1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazol-4-ylmethyl]-(1-methyl-1H-imidazol-2-ylmethyl)-amino]-methyl}-nicotinic acid 
• 675583-73-0 [1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazol-4-ylmethyl]-(1-methyl-1H-imidazol-2-ylmethyl)-amine 
• 854779-50-3 [1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazol-4-yl]-methanol 
• 675583-72-9 1-(2-methoxymethoxy-5-methyl-phenyl)-1H-imidazole-4-carbaldehyde 

Relevant academic research and scientific papers

Hexaphenolic Rigid Cages Prepared by Self-Organization of C 3v Tridentates

Coordination cages were composed by self-organization of rigid C3v-symmetric heptaarene tridentates and Pd(II) precursors. The heptaarene framework involves one mesitylene, three phenol, and three pyridine moieties, which were connected by Suzu

Bacterial Catabolism of Biphenyls: Synthesis and Evaluation of Analogues

A series of alkylated 2,3-dihydroxybiphenyls has been prepared on the gram scale by using an effective Directed ortho Metalation–Suzuki–Miyaura cross-coupling strategy. These compounds have been used to investigate the substrate specificity of the meta-cl

Synthetic models of the active site of cytochrome c oxidase: Influence of tridentate or tetradentate copper chelates bearing a his-tyr linkage mimic on dioxygen adduct formation by heme/cu complexes

Two synthetic models of the active site of cytochrome c oxidase-[(L N4-OH)CuI-FeII(TMP)]+ (1a) and [(LN3-OH)CuI-FeII(TMP)]+ (2a)-have been designed and synthesized. These models

Formation and spectroscopic characterization of the dioxygen adduct of a heme-Cu complex possessing a cross-linked tyrosine-histidine mimic: modeling the active site of cytochrome c oxidase.

A binucleating porphyrin with covalently appended copper chelates having a cross-linked imidazole-phenol group as the novel active site model of cytochrome c oxidase has been prepared, and the dioxygen adduct of its iron(II)-copper(I) complex was spectros