Product Name:5-Methylpyrimidin-2(1H)-one

IUPAC Name:5-methyl-1,2-dihydropyrimidin-2-one

CAS:41398-85-0
Molecular Formula:C5H6N2O
Purity:95%
Catalog Number:CM166741
Molecular Weight:110.12

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CM166741-250mg in stock ƎƎNJ
CM166741-1g in stock ưȁț
CM166741-5g 1-2 Weeks ȁțǜ

For R&D use only.

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Product Details

CAS NO:41398-85-0
Molecular Formula:C5H6N2O
Melting Point:-
Smiles Code:CC1=CNC(=O)N=C1
Density:
Catalog Number:CM166741
Molecular Weight:110.12
Boiling Point:309.1°C at 760 mmHg
MDL No:MFCD09991915
Storage:Store at 2-8°C.

Category Infos

Pyrimidines
Pyrimidine, also known as 1,3-diazobenzene, is a heterocyclic compound with the chemical formula C4H4N2. Pyrimidine is formed by substituting 2 nitrogen atoms for 2 carbons in the meta-position of benzene. It is a diazine and retains its aromaticity. Derivatives of pyrimidine widely exist in organic macromolecular nucleic acids, and many drugs also contain pyrimidine rings. In nucleic acids, three nucleobases are pyrimidine derivatives: cytosine, thymine and uracil. There are a variety of pyrimidine-containing drugs on the market, most of which are kinase inhibitors.

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Product Other Information

Product Overview 2-Hydroxy-5-methylpyrimidine is a heterocyclic organic compound with a molecular formula of C5H6N2O. It is a colorless solid that is soluble in water and alcohol. It is a common intermediate in the synthesis of many important drugs, such as anti-inflammatory drugs, antibiotics, and anti-cancer drugs. It is also used in the synthesis of other pharmaceuticals, such as vitamins and anti-fungal agents. 2-Hydroxy-5-methylpyrimidine is an important precursor for the synthesis of a wide range of compounds, including pyrimidines, purines, and other heterocyclic compounds.
Synthesis and Application 2-Hydroxy-5-methylpyrimidine can be synthesized by a variety of methods. The most common method is the reaction of 2-amino-5-methylpyrimidine with aqueous hydrochloric acid. This reaction is typically carried out at room temperature and results in the formation of 2-hydroxy-5-methylpyrimidine and water. Other methods of synthesis include the reaction of 2-amino-5-methylpyrimidine with ethyl alcohol and the reaction of 2-amino-5-methylpyrimidine with acetic anhydride. 2-Hydroxy-5-methylpyrimidine has a wide range of scientific research applications. It is used in the synthesis of a variety of pharmaceuticals, including anti-inflammatory drugs, antibiotics, and anti-cancer drugs. It is also used in the synthesis of other heterocyclic compounds, such as pyrimidines, purines, and other heterocyclic compounds. In addition, it is used in the synthesis of organic pigments and dyes.
Future Directions The potential future directions for the use of 2-Hydroxy-5-methylpyrimidine in scientific research include its use in the synthesis of new pharmaceuticals, its use in the synthesis of organic pigments and dyes, and its use in the development of new drugs and therapies. Additionally, its potential antioxidant activity could be explored further, and its potential toxicity could be studied in more detail. Its potential use in the development of new drugs and therapies could also be studied, and its potential use in the synthesis of new pharmaceuticals could be explored.