58418-62-5

Basic information

• Product Name: 3-(Methoxymethyl)pyridine
• Synonyms: 3-(Methoxymethyl)pyridine
• CAS NO: 58418-62-5
• Molecular Formula: C₇H₉NO
• Molecular Weight: 123.15246
• Mol File: 58418-62-5.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 177.6 °C at 760 mmHg
• Flash Point: 62.8 °C
• Appearance: /
• Density: 1.01 g/cm³
• Vapor Pressure: 1.39mmHg at 25°C
• Refractive Index: 1.496
• CAS DataBase Reference: 3-(Methoxymethyl)pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(Methoxymethyl)pyridine(58418-62-5)
• EPA Substance Registry System: 3-(Methoxymethyl)pyridine(58418-62-5)

Safety Data

• Hazardous Substances Data: 58418-62-5(Hazardous Substances Data)

Usage

General Description

3-(Methoxymethyl)pyridine is a chemical compound that belongs to the class of organic compounds known as pyridines. 3-(methoxymethyl)pyridine has a molecular formula of C7H9NO and a molecular weight of 121.151 grams per mol. It can be identified by its systematic name - Picoline, 3-(methoxymethyl), which indicates its structure, i.e., a pyridine ring with a methoxymethyl group at the 3rd position. This chemical exhibits a strong smell and is typically used in research applications, particularly in the field of chemistry for the synthesis of various other compounds. However, its potential hazards must be taken into consideration as it can be harmful if inhaled, swallowed or in case of skin contact.

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

Downstream Products

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

Relevant articles and documents

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.

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.