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5-ACETYL-2-METHOXYPYRIDINE, 97% CAS:213193-32-9

5-Acetyl-2-methoxypyridine is an organic compound with the molecular formula C8H9NO2. It features a pyridine ring substituted with an acetyl group at the 5-position and a methoxy group at the 2-position. This molecule exhibits interesting electronic characteristics due to the presence of both electron-donating (methoxy) and electron-withdrawing (acetyl) groups, influencing its reactivity in various chemical processes. The compound holds significance in organic synthesis, particularly as a building block for pharmaceuticals and agrochemicals. Its versatile reactivity enables diverse transformations, making it a valuable intermediate in synthetic chemistry and research into new biologically active compounds.

 


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Application and Effect:

5-Acetyl-2-methoxypyridine is a noteworthy organic compound characterized by its specific substitution pattern on the pyridine ring, which significantly influences its electronic and chemical properties. With the molecular formula C8H9NO2, this compound comprises a pyridine core bearing an acetyl group at the 5-position and a methoxy group at the 2-position. This arrangement imparts distinct electrophilic and nucleophilic characters, enhancing the compound's utility in organic synthesis. The acetyl group serves as an electron-withdrawing moiety, while the methoxy group provides electron-donating capabilities. This combination leads to a polarized electronic environment, making 5-acetyl-2-methoxypyridine a reactive species in various chemical reactions. For instance, it can undergo nucleophilic substitutions, electrophilic aromatic substitutions, and condensation reactions. Such versatility makes it a valuable intermediate in the synthesis of diverse organic compounds. In the pharmaceutical industry, 5-acetyl-2-methoxypyridine has gained interest as a precursor for developing bioactive molecules. Compounds derived from this structure may exhibit significant biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Research into the structure-activity relationships (SAR) of these derivatives can lead to the discovery of new therapeutic agents that address unmet medical needs. Additionally, the compound's unique architecture makes it relevant in materials science. It can be utilized as a building block for synthesizing functional materials, such as polymers and dyes, expanding its applicability beyond traditional organic synthesis. Overall, 5-acetyl-2-methoxypyridine illustrates the importance of functionalized pyridine derivatives in modern organic chemistry. Its reactivity and potential bioactivity continue to drive research aimed at discovering innovative compounds, ultimately contributing to advancements in drug development and material science. The ongoing exploration of this compound’s properties and applications underscores its value in contemporary chemical research.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C6H8ClN
Assay 99%
Appearance white powder
CAS No.  213193-32-9
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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