Nom du produit:7-Hydroxy-5,6-dimethylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid

IUPAC Name:7-hydroxy-5,6-dimethylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid

CAS:1284618-26-3
Formule moléculaire:C9H9N3O3
Pureté:97%
Numéro de catalogue:CM287421
Poids moléculaire:207.19

Unité d'emballage Stock disponible Prix($) Quantité
CM287421-1g 3-4 Weeks Ȑŵŵ
CM287421-5g 3-4 Weeks ȺȺȺ
CM287421-10g 3-4 Weeks ƛȐƥǜ

Pour une utilisation en R&D uniquement..

Formulaire de demande

   refresh    

Détails du produit

N° CAS:1284618-26-3
Formule moléculaire:C9H9N3O3
Point de fusion:-
Code SMILES:O=C(C1=C2N=C(C)C(C)=C(O)N2N=C1)O
Densité:
Numéro de catalogue:CM287421
Poids moléculaire:207.19
Point d'ébullition:
N° Mdl:
Stockage:

Category Infos

Pyrazolopyrimidines
Pyrazolopyrimidine scaffolds are one of the most important heterocyclic compounds in drug discovery. This scaffold has various biological activities, among which anticancer is an important one.

Related Products



Product Other Information

Product Overview 7-Hydroxy-5,6-dimethylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid (DPC) is a heterocyclic compound that has been widely studied for its potential applications in various fields of science. It is an isomer of 7-hydroxy-6-methylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid (MPC) and has a similar chemical structure. DPC has been found to exhibit a range of biochemical and physiological effects, making it a promising candidate for further research.
Synthesis and Application DPC can be synthesized through a number of methods, including the reaction between 5,6-dimethylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid and hydroxylamine-O-sulfonic acid, followed by oxidation with potassium permanganate. Another method involves the reaction between 5,6-dimethylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid and hydroxylamine hydrochloride, followed by oxidation with sodium periodate. 7-Hydroxy-5,6-dimethylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid has been extensively studied for its potential applications in various fields of science, including medicinal chemistry, pharmacology, and biochemistry. It has been found to exhibit a range of biological activities, such as anti-inflammatory, antioxidant, and antimicrobial properties. 7-Hydroxy-5,6-dimethylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid has also been shown to have potential applications in the treatment of various diseases, including cancer, diabetes, and neurodegenerative disorders.
Future Directions There are several future directions for research on 7-Hydroxy-5,6-dimethylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid, including the development of new synthetic methods, the investigation of its mechanism of action, and the exploration of its potential applications in various fields of science. One possible direction for research is the development of more efficient synthetic methods for 7-Hydroxy-5,6-dimethylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid, which may allow for the production of larger quantities of the compound. Another direction for research is the investigation of the mechanism of action of 7-Hydroxy-5,6-dimethylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid, which may provide insights into its biological activities and potential applications. Additionally, further research is needed to explore the potential applications of 7-Hydroxy-5,6-dimethylpyrazolo[1,5-a]pyrimidine-3-carboxylic acid in the treatment of various diseases, such as cancer, diabetes, and neurodegenerative disorders.