58418-62-5

Usage

Uses

Used in Chemical Research:
3-(Methoxymethyl)pyridine is used as a synthetic intermediate for the preparation of various other compounds in the field of chemistry. Its unique structure, featuring a pyridine ring with a methoxymethyl group at the 3rd position, makes it a valuable building block for the development of new chemical entities.
Used in Pharmaceutical Industry:
3-(Methoxymethyl)pyridine is used as a key component in the synthesis of certain pharmaceutical compounds. Its versatility in chemical reactions allows for the creation of potential drug candidates, contributing to the advancement of medicinal chemistry.
Used in Material Science:
3-(Methoxymethyl)pyridine is used as a precursor in the development of new materials with specific properties, such as improved stability or reactivity. Its incorporation into the molecular structure of these materials can lead to enhanced performance in various applications.

InChI:InChI=1/C7H9NO/c1-9-6-7-3-2-4-8-5-7/h2-5H,6H2,1H3

Upstream product

• 100-55-0 3-hydroxymethylpyridin 
• 124-41-4 sodium methylate 
• 6959-48-4 3-chloromethylpyridinium chloride 
• 108-99-6 3-Methylpyridine 
• 74-88-4 methyl iodide 

Downstream Products

• 191332-29-3 4-benzyl-3-methoxymethylpyridine 
• 500-22-1 3-pyridinecarboxaldehyde 
• 191332-30-6 4-Benzyl-3-methoxymethyl-1,2,5,6-tetrahydropyridine Hydrochloride 
• 1282541-12-1 N-[2-hydroxy-5-(trifluoromethyl)phenyl]-3-(methoxymethyl)isonicotinamide 

Relevant academic research and scientific papers

HETEROCYCLIC COMPOUNDS AND USES THEREOF

Provided herein are novel heterocyclic compounds, for example, compounds having Formula I, I-P, II, lI-P, or III. Also provided herein are pharmaceutical compositions comprising the compounds and methods of using the same, for example, in inhibiting aldehyde dehydrogenases and/or for treating various cancers, cancer metastasis, type 2 diabetes, pulmonary arterial hypertension (PAH) or neointimal hyperplasia (NIH).

Merging Photoredox with Br?nsted Acid Catalysis: The Cross-Dehydrogenative C?O Coupling for sp3 C?H Bond Peroxidation

A photoredox and Br?nsted acid synergistically catalyzed cross-dehydrogenative C?O coupling reaction is developed in which isochroman peroxyacetals are formed through sp3 C?H bond peroxidation. The reported method is characterized by its extremely mild reaction conditions, excellent yields, and broad substrate scope. An oxocarbenium ion p-chlorobenzenesulfonate was speculated to be the reactive intermediate. The role of hemiacetals and oxygenated dimers on the effective stabilization of the oxocarbenium ion was investigated; the presence of acid appeared to establish equilibrium between hemiacetals and oxygenated dimers with the oxocarbenium ion pairs. The broad applicability of the method highlights the potential of the protocol for molecule synthesis.

Synthetic method of 3-methoxymethylpyridine

The invention relates to the field of organic chemistry, in particular to a synthetic method of 3-methoxymethylpyridine. The synthetic method comprises the following steps: using 3-methylpyridine as a raw material, and carrying out bromination reaction to obtain 3-bromo-methylpyridine; reacting the 3-bromo-methylpyridine with trimethylamine to obtain (3-picolyl) trimethyl ammonium bromide; dissolving the (3-picolyl) trimethyl ammonium bromide into methanol, then adding sodium methylate, and carrying out heating reflux in the presence of nitrogen for 1 hour to obtain the 3-methoxymethylpyridine. By adopting the synthetic method disclosed by the invention, the 3-methylpyridine is used as the raw material and is subjected to the bromination reaction to obtain the 3-bromo-methylpyridine; the 3-bromo-methylpyridine reacts with the trimethylamine to obtain the (3-picolyl) trimethyl ammonium bromide; finally, the (3-picolyl) trimethyl ammonium bromide reacts with the sodium methoxide to obtain the 3-methoxymethylpyridine. The synthetic method disclosed by the invention has the advantages of high total yield, low price of raw materials, short reaction time, mild conditions and simple process operation.

HARMFUL ARTHROPOD CONTROL COMPOSITION, AND FUSED HETEROCYCLIC COMPOUND

Disclosed is a harmful arthropod control composition comprising, as an active ingredient, a fused heterocyclic compound represented by formula (1) [wherein A1 and A2 independently represent a nitrogen atom or the like; R1 and R4 independently represent a halogen atom or the like; R2 and R3 independently represent a halogen atom or the like; R5 and R6 independently represent a linear C1-C6 hydrocarbon group which may be substituted, or the like (provided that both R5 and R6 cannot represent a hydrogen atom simultaneously); and n represents 0 or 1]. The harmful arthropod control composition has an excellent efficacy to control harmful arthropods.

HARMFUL ARTHROPOD CONTROL COMPOSITION, AND FUSED HETEROCYCLIC COMPOUND

Disclosed is a harmful arthropod control composition comprising, as an active ingredient, a fused heterocyclic compound represented by formula (1) [wherein A1 and A2 independently represent a nitrogen atom or the like; R1 and R4 independently represent a halogen atom or the like; R2 and R3 independently represent a halogen atom or the like; R5 and R6 independently represent a linear C1-C6 hydrocarbon group which may be substituted, or the like (provided that both R5 and R6 cannot represent a hydrogen atom simultaneously); and n represents 0 or 1]. The harmful arthropod control composition has an excellent efficacy to control harmful arthropods.

COMPOSITION AND METHOD FOR CONTROLLING ARTHROPOD PESTS

The present invention provides: an arthropod pests control composition comprising, as active ingredients, a condensed heterocyclic compound and a neonicotinoid compound; a method for controlling arthropod pests which comprises applying effective amounts of a condensed heterocyclic compound and a neonicotinoid compound to the arthropod pests or a locus where the arthropod pests inhabit; and so on.

COMPOSITION AND METHOD FOR CONTROLLING ARTHROPOD PESTS

The present invention provides: an arthropod pests control composition comprising, as active ingredients, a condensed heterocyclic compound and pyriproxyfen; a method for controlling arthropod pests which comprises applying effective amounts of a condensed heterocyclic compound and pyriproxyfen to the arthropod pests or a locus where the arthropod pests inhabit; and so on.

COMPOSITION AND METHOD FOR CONTROLLING ARTHROPOD PESTS

The present invention provides: an arthropod pests control composition comprising, as active ingredients, a condensed heterocyclic compound and a pyrethroid compound; a method for controlling arthropod pests which comprises applying effective amounts of a condensed heterocyclic compound and a pyrethroid compound to the arthropod pests or a locus where the arthropod pests inhabit; and so on.

COMPOSITION AND METHOD FOR CONTROLLING ARTHROPOD PESTS

The present invention provides: an arthropod pests control composition comprising, as active ingredients, a condensed heterocyclic compound and pyridalyl; a method for controlling arthropod pests which comprises applying effective amounts of a condensed heterocyclic compound and pyridalyl to the arthropod pests or a locus where the arthropod pests inhabit; and so on.

COMPOSITION AND METHOD FOR CONTROLLING ARTHROPOD PESTS

The present invention provides: an arthropod pests control composition comprising, as active ingredients, a condensed heterocyclic compound and a diamide compound; a method for controlling arthropod pests which comprises applying effective amounts of a condensed heterocyclic compound and a diamide compound to the arthropod pests or a locus where the arthropod pests inhabit; and so on.