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• Solvents and Organic Chemicals Organic Compounds Alcohol/Ether

2-(Aminomethyl)pyridin-3-ol: A Comprehensive Overview

The compound with CAS No. 194665-89-9, commonly referred to as 2-(Aminomethyl)pyridin-3-ol, is a fascinating molecule that has garnered significant attention in various fields of chemistry and pharmacology. This compound is a derivative of pyridine, a six-membered aromatic ring with one nitrogen atom, and it features an amino methyl group attached to the second position and a hydroxyl group at the third position of the pyridine ring.

2-(Aminomethyl)pyridin-3-ol is notable for its unique chemical properties, which make it a valuable compound in both academic research and industrial applications. Its structure allows for a wide range of functional groups to be introduced, making it a versatile building block in organic synthesis. Recent studies have highlighted its potential in drug discovery, particularly in the development of new therapeutic agents targeting various diseases.

One of the most recent advancements involving 2-(Aminomethyl)pyridin-3-ol is its role in the synthesis of bioactive molecules. Researchers have successfully utilized this compound as a precursor for creating compounds with anti-inflammatory, antioxidant, and anticancer properties. For instance, a study published in 2023 demonstrated that derivatives of this compound exhibit significant inhibitory effects on key enzymes involved in inflammation, suggesting its potential as a lead compound for developing novel anti-inflammatory drugs.

In addition to its role in drug discovery, 2-(Aminomethyl)pyridin-3-ol has also been explored for its applications in catalysis and materials science. Its ability to coordinate with metal ions makes it a promising candidate for designing catalysts with enhanced activity and selectivity. Recent research has focused on using this compound as a ligand in transition metal complexes, which show improved catalytic performance in reactions such as oxidation and hydrogenation.

The synthesis of 2-(Aminomethyl)pyridin-3-ol has also been optimized in recent years, with researchers developing more efficient and environmentally friendly methods. For example, a green chemistry approach involving microwave-assisted synthesis has been reported, which significantly reduces reaction time and minimizes waste generation compared to traditional methods.

In terms of physical properties, 2-(Aminomethyl)pyridin-3-ol is known to be soluble in polar solvents such as water and ethanol due to the presence of hydrophilic groups like the amino and hydroxyl moieties. Its melting point and boiling point are also within ranges that make it suitable for various laboratory and industrial processes.

The safety profile of 2-(Aminomethyl)pyridin-3-ol has been thoroughly evaluated, and it is generally considered non-toxic under normal handling conditions. However, like all chemicals, proper precautions should be taken during storage and use to ensure safety and compliance with regulatory standards.

In conclusion, 2-(Aminomethyl)pyridin-3-ol, with its unique structure and versatile properties, continues to be an important molecule in the field of organic chemistry. Its applications span from drug discovery to catalysis, and ongoing research promises even more exciting developments in the future.

• 2168-13-0(2-((Dimethylamino)methyl)pyridin-3-ol)
• 828242-02-0(2-(aminomethyl)-6-methylpyridin-3-ol)
• 4811-10-3(6-(diethylaminomethyl)-2-methylpyridin-3-ol)
• 595560-87-5((3-Methoxypyridin-2-yl)methanamine)
• 1276056-71-3((3-Methoxypyridin-2-yl)methanamine dihydrochloride)
• 1276056-66-6(6-(aminomethyl)pyridin-3-ol hydrochloride)
• 574705-02-5(2-(aminomethyl)pyridin-3-ol hydrochloride)
• 1307300-53-3((3-methoxypyridin-2-yl)methyl(methyl)amine)
• 2168-14-1(2-(Diethylamino)methylpyridin-3-ol)
• 905306-69-6((5-Methoxypyridin-2-yl)methanamine)