Product Name:5-Amino-3-methylpyridin-2-ol

IUPAC Name:5-amino-3-methylpyridin-2-ol

CAS:20252-07-7
Molecular Formula:C6H8N2O
Purity:95%
Catalog Number:CM314937
Molecular Weight:124.14

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CM314937-1g 1-2 Weeks Ťľƈ

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Product Details

CAS NO:20252-07-7
Molecular Formula:C6H8N2O
Melting Point:-
Smiles Code:OC1=NC=C(N)C=C1C
Density:
Catalog Number:CM314937
Molecular Weight:124.14
Boiling Point:
MDL No:MFCD07375119
Storage:

Category Infos

Pyridines
Pyridine is a six-membered heterocyclic compound containing one nitrogen heteroatom. Pyridine and piperidine are the most frequently occurring heterocyclic building blocks in drug molecules. According to incomplete statistics, there are currently more than 180 drugs containing pyridine or piperidine structure that have been marketed, nearly 1/5 of the drugs approved for marketing in recent years contain these two structures.
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Pyridine is a basic heterocyclic organic compound with the chemical formula C5H5N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom. It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell.

Product Other Information

Product Overview 5-Amino-3-methylpyridin-2-ol, also known as AMP2, is a synthetic organic compound that has gained attention in recent years due to its potential applications in various scientific fields. AMP2 is a white crystalline solid with a molecular weight of 124.14 g/mol and a melting point of 99-102°C. It is most commonly used as a starting material for the synthesis of various organic compounds and as a reagent in chemical reactions. This compound has also been studied for its potential in biomedical applications, such as drug delivery, enzyme inhibition, and gene regulation.
Synthesis and Application 5-Amino-3-methylpyridin-2-ol can be synthesized in a number of different ways, but the most common method is the Fischer indole synthesis. This method involves the condensation of an aromatic aldehyde and an amine, followed by a dehydration reaction to form the desired product. The reaction can be carried out in either an aqueous or an organic solvent, and the reaction conditions can be adjusted to optimize the yield. Other methods for the synthesis of 5-Amino-3-methylpyridin-2-ol include the Biginelli reaction, the Knoevenagel condensation, and the Ugi reaction. 5-Amino-3-methylpyridin-2-ol has been studied extensively for its potential applications in various scientific fields. In particular, it has been used as a starting material in the synthesis of various organic compounds, such as pharmaceuticals, agrochemicals, and dyes. Additionally, it has been studied for its potential use in drug delivery, enzyme inhibition, and gene regulation. It has also been used in the development of new materials, such as polymers, catalysts, and nanomaterials.
Future Directions There are many potential future directions for the use of 5-Amino-3-methylpyridin-2-ol. It could be used to develop new drugs or to improve existing drugs. Additionally, it could be used to study the effects of cellular stress and the regulation of gene expression. Additionally, it could be used to develop new materials, such as polymers, catalysts, and nanomaterials. Finally, it could be used to study the mechanisms of enzyme inhibition and drug delivery.