Produktname:ethyl 3-bromopyrazolo[1,5-a]pyrimidine-6-carboxylate
IUPAC Name:ethyl 3-bromopyrazolo[1,5-a]pyrimidine-6-carboxylate
| Packungseinheit | Verfügbarer Vorrat | Preis($) | Menge |
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| CM104134-100mg | in stock | ƋƋƋ |
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| CM104134-250mg | in stock | ƋƼDz |
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| CM104134-1g | in stock | ſdždž |
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| Product Overview |
ethyl 3-bromopyrazolo[1,5-a]pyrimidine-6-carboxylate (EBPC) is a synthetic compound with a wide range of applications in scientific research. It is a brominated pyrazolo[1,5-a]pyrimidine derivative, which is a heterocyclic compound containing nitrogen, carbon, and bromine atoms. EBPC has been studied for its potential uses in organic synthesis, biochemistry, and pharmacology. |
| Synthesis and Application |
ethyl 3-bromopyrazolo[1,5-a]pyrimidine-6-carboxylate is synthesized from ethyl 3-bromopyrazole-5-carboxylate (EBC) and ethyl 3-amino-5-methylpyrazole-4-carboxylate (EAMPC). The synthesis of ethyl 3-bromopyrazolo[1,5-a]pyrimidine-6-carboxylate is carried out in two steps. In the first step, EBC is reacted with sodium ethoxide in ethanol to form ethyl 3-bromo-5-hydroxy-pyrazole-4-carboxylate (EBHPC). In the second step, EBHPC is reacted with EAMPC in the presence of pyridine and acetic acid to form ethyl 3-bromopyrazolo[1,5-a]pyrimidine-6-carboxylate. The overall yield of ethyl 3-bromopyrazolo[1,5-a]pyrimidine-6-carboxylate is approximately 70%. ethyl 3-bromopyrazolo[1,5-a]pyrimidine-6-carboxylate has a wide range of applications in scientific research. It has been used as a reagent in organic synthesis, as a ligand in coordination chemistry, and as a catalyst in catalytic hydrogenation. It has also been used in the synthesis of other heterocyclic compounds, such as imidazoles, pyrazolines, and pyrimidines. In addition, ethyl 3-bromopyrazolo[1,5-a]pyrimidine-6-carboxylate has been used in the synthesis of biologically active compounds, such as antibiotics, antivirals, and antifungals. |
| Future Directions |
There are several possible future directions for research on ethyl 3-bromopyrazolo[1,5-a]pyrimidine-6-carboxylate. These include further investigation of its potential effects on biochemical and physiological processes, such as its effects on gene expression and cell cycle regulation. Other areas of research could include its use as a catalyst in organic synthesis and its potential applications in drug discovery. In addition, further studies could be conducted to determine the mechanism of action of ethyl 3-bromopyrazolo[1,5-a]pyrimidine-6-carboxylate and to explore its potential therapeutic applications. |
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