6-Amino-2-methylphenol (CAS 17672-22-9): A Deep Dive into its Chemical Significance
The intricate world of chemistry often hinges on the specific functionalities and arrangement of atoms within a molecule. 6-Amino-2-methylphenol, identified by its CAS number 17672-22-9, is a compound whose chemical significance stems from its unique structure and the reactivity it affords. NINGBO INNO PHARMCHEM CO.,LTD. provides insights into the chemical importance of this versatile compound.
At its core, 6-Amino-2-methylphenol possesses the molecular formula C7H9NO. The benzene ring forms the structural backbone, substituted with three key functional groups: an amino group (-NH2), a hydroxyl group (-OH), and a methyl group (-CH3). The ortho-positioning of the hydroxyl and methyl groups, and the para-positioning of the amino group relative to the methyl, contribute to its specific reactivity and physical properties, such as being a colorless liquid with a high purity assay of 99.0%min.
The presence of both a nucleophilic amino group and a phenolic hydroxyl group makes 6-Amino-2-methylphenol a bifunctional molecule, capable of undergoing a wide array of chemical transformations. The amino group can readily react with electrophiles, undergo acylation, or participate in condensation reactions. The phenolic hydroxyl group can be alkylated, acylated, or involved in oxidation reactions. These dual reactivities are what make it an exceptionally valuable intermediate in complex organic syntheses, whether for pharmaceutical drugs, agrochemicals, or specialized fine chemicals.
The structure-activity relationship is particularly noteworthy. The electronic effects of the substituents on the aromatic ring influence the reactivity of each functional group. For instance, the electron-donating nature of the amino and methyl groups can activate the ring towards electrophilic aromatic substitution. Understanding these nuances is critical for chemists who aim to buy 6-amino-2-methylphenol for targeted synthetic outcomes.
From a manufacturing standpoint, achieving the high purity of 99.0%min requires precise control over the synthesis process. Suppliers like NINGBO INNO PHARMCHEM CO.,LTD. invest heavily in advanced manufacturing techniques and quality control to ensure that the compound meets the demanding standards of industries such as pharmaceuticals, which often require adherence to USP, BP, and EP specifications.
The significance of 6-Amino-2-methylphenol extends beyond its direct use as a reactant; it can also serve as a precursor for ligands, catalysts, or building blocks for more complex molecular architectures. Its consistent availability and competitive price from Chinese manufacturers further enhance its appeal in the global chemical market.
NINGBO INNO PHARMCHEM CO.,LTD. is proud to supply 6-Amino-2-methylphenol, a compound whose chemical significance is deeply rooted in its versatile structure. We are committed to providing the chemical industry with high-quality intermediates that drive innovation and scientific advancement.
Perspectives & Insights
Agile Reader One
“The amino group can readily react with electrophiles, undergo acylation, or participate in condensation reactions.”
Logic Vision Labs
“The phenolic hydroxyl group can be alkylated, acylated, or involved in oxidation reactions.”
Molecule Origin 88
“These dual reactivities are what make it an exceptionally valuable intermediate in complex organic syntheses, whether for pharmaceutical drugs, agrochemicals, or specialized fine chemicals.”