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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Pyridinecarboxamides
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Pyridinecarboxylic acids and derivatives Pyridinecarboxamides

Introduction to CAS No. 145255-19-2: 5-Aminopyridine-2-carboxamide

CAS No. 145255-19-2, commonly referred to as 5-Aminopyridine-2-carboxamide, is a compound of significant interest in the fields of organic chemistry and pharmaceutical research. This compound belongs to the class of pyridine derivatives, which are widely studied for their diverse applications in drug design, agrochemicals, and materials science. The structure of 5-Aminopyridine-2-carboxamide consists of a pyridine ring with an amino group at position 5 and a carboxamide group at position 2, making it a versatile scaffold for further functionalization.

The synthesis of CAS No. 145255-19-2 involves a series of well-established organic reactions, including nucleophilic substitutions and amide bond formations. Recent advancements in catalytic methods have enabled the efficient and selective synthesis of this compound, reducing production costs and improving yield. Researchers have also explored the use of microwave-assisted synthesis and continuous flow reactors to optimize the production process, aligning with the growing demand for sustainable chemical manufacturing practices.

5-Aminopyridine-2-carboxamide has demonstrated potential in several therapeutic areas. For instance, studies have shown that this compound exhibits inhibitory activity against certain enzymes involved in inflammatory pathways, making it a promising candidate for anti-inflammatory drug development. Additionally, its ability to modulate ion channels has been explored in the context of treating neurological disorders such as epilepsy and chronic pain.

In the agricultural sector, CAS No. 145255-19-2 has been investigated for its potential as a herbicide or fungicide. Recent research highlights its effectiveness in inhibiting key enzymes responsible for plant pathogen growth, suggesting its role in developing eco-friendly crop protection agents. Moreover, the compound's stability under various environmental conditions makes it suitable for field applications.

The pharmacokinetic properties of 5-Aminopyridine-2-carboxamide have been extensively studied to evaluate its bioavailability and metabolic profile. Preclinical studies indicate that the compound exhibits moderate absorption rates and favorable distribution characteristics, which are critical factors for its potential use as an orally administered drug. Furthermore, its metabolic pathways have been mapped using advanced metabolomics techniques, providing insights into its safety profile and toxicity mechanisms.

Recent breakthroughs in computational chemistry have enabled researchers to predict the binding affinities of CAS No. 145255-19-2 with various biological targets with high accuracy. Machine learning algorithms have been employed to identify novel targets for this compound, expanding its potential applications beyond traditional therapeutic areas. These computational approaches not only accelerate drug discovery but also reduce the reliance on time-consuming experimental methods.

In conclusion, CAS No. 145255-19-2 (5-Aminopyridine-2-carboxamide) stands out as a multifaceted compound with promising applications across multiple industries. Its unique chemical structure, coupled with advancements in synthetic methodologies and computational tools, positions it as a valuable asset in both academic research and industrial development.

• 1121-60-4(pyridine-2-carbaldehyde)
• 1462-86-8(3-aminopyridine-2-carboxylic acid)
• 5112-36-7(Pyridine 2,6-dicarboxylicdihydrazide)
• 3731-51-9(1-(pyridin-2-yl)methanamine)
• 3430-33-9(2,6-Dimethylpyridin-3-amine)
• 4329-81-1(Phenyl-pyridin-2-ylmethyl-amine)
• 50608-99-6(3-Aminopyridine-2-carboxamide)
• 4664-00-0(Quinolinimide)
• 3430-10-2(3-Amino-2-methylpyridine)
• 3430-14-6(5-Amino-2-picoline)