Cas no 20027-70-7 (4-(methoxymethyl)pyridine)

4-(methoxymethyl)pyridine structure
4-(methoxymethyl)pyridine structure
Product Name:4-(methoxymethyl)pyridine
CAS No:20027-70-7
MF:C7H9NO
MW:123.152461767197
CID:860497
Update Time:2026-04-29

4-(methoxymethyl)pyridine Chemical and Physical Properties

Names and Identifiers

    • 4-(methoxymethyl)pyridine

Computed Properties

  • Exact Mass: 123.06847

Experimental Properties

  • PSA: 22.12

4-(methoxymethyl)pyridine Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
1PlusChem
1P00BFYX-1g
1/C7H9NO/c1-9-6-7-2-4-8-5-3-7/h2-5H,6H2,1H
20027-70-7 ≥ 98% (GC)
1g
$116.00 2023-12-19
A2B Chem LLC
AF33113-1g
1/C7H9NO/c1-9-6-7-2-4-8-5-3-7/h2-5H,6H2,1H
20027-70-7 ≥ 98% (GC)
1g
$91.00 2024-04-20

Additional information on 4-(methoxymethyl)pyridine

Comprehensive Overview of 4-(Methoxymethyl)pyridine (CAS No. 20027-70-7): Properties, Applications, and Industry Insights

4-(Methoxymethyl)pyridine (CAS No. 20027-70-7) is a specialized organic compound that has garnered significant attention in pharmaceutical, agrochemical, and material science research. This heterocyclic derivative, featuring a pyridine ring substituted with a methoxymethyl group, exhibits unique chemical properties that make it valuable for synthetic applications. Its molecular formula, C7H9NO, and moderate polarity contribute to its versatility in organic synthesis.

In recent years, the demand for 4-(Methoxymethyl)pyridine has surged due to its role as a key intermediate in the production of pharmaceutical APIs (Active Pharmaceutical Ingredients) and crop protection agents. Researchers frequently search for "synthesis of 4-(Methoxymethyl)pyridine" or "CAS 20027-70-7 solubility data," reflecting the compound's technical relevance. The methoxymethyl moiety enhances the molecule's reactivity, enabling its use in cross-coupling reactions and N-alkylation processes.

From an industrial perspective, 4-(Methoxymethyl)pyridine aligns with the growing focus on green chemistry and sustainable synthesis. Its potential as a bio-based intermediate has been explored in peer-reviewed studies, addressing concerns about environmental impact in chemical manufacturing. Analytical techniques like HPLC purity testing and GC-MS characterization are commonly employed to ensure quality control for this compound.

The compound's physicochemical properties—including a boiling point of ~210°C and logP value of 0.89—make it suitable for solvent-mediated reactions. Safety data sheets emphasize proper handling procedures, though it doesn't fall under hazardous classifications. Users often inquire about "4-(Methoxymethyl)pyridine storage conditions" or "compatible materials for CAS 20027-70-7," highlighting practical usage considerations.

Emerging applications in electronic materials have expanded the market for 20027-70-7, particularly in OLED precursor synthesis and conductive polymer development. Patent literature reveals innovative uses in photocatalysis and coordination chemistry, where its nitrogen donor capability proves advantageous. The compound's regioselectivity in reactions remains a focal point for methodological improvements.

Quality benchmarks for 4-(Methoxymethyl)pyridine typically require ≥98% purity, with stringent control of pyridine derivatives and process impurities. Analytical certificates often include NMR spectra and residual solvent analysis to verify composition. The compound's stability under nitrogen atmosphere and compatibility with anhydrous conditions are frequently documented in technical bulletins.

Market analysts note increasing custom synthesis requests for CAS 20027-70-7, driven by drug discovery pipelines and specialty chemical development. The compound's scalability in production and cost-effectiveness compared to analogous heterocyclic building blocks contribute to its commercial viability. Regulatory compliance with REACH and FDA guidelines ensures its global accessibility for research purposes.

Future research directions may explore enantioselective applications of 4-(Methoxymethyl)pyridine or its derivatives in asymmetric catalysis. The compound's structure-activity relationships continue to be investigated for potential biological activity modulation. With proper intellectual property strategies, novel applications in material science and medicinal chemistry are expected to emerge in coming years.

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