CAS 13877-56-0
:1H-Pyrazolo[4,3-d]pyrimidin-7-amine
Description:
1H-Pyrazolo[4,3-d]pyrimidin-7-amine is a heterocyclic organic compound characterized by a fused pyrazole and pyrimidine ring system. This compound features an amino group at the 7-position of the pyrimidine ring, which contributes to its reactivity and potential biological activity. It is typically a crystalline solid and may exhibit solubility in polar organic solvents. The presence of the pyrazole and pyrimidine moieties suggests that it may interact with biological targets, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The compound's structure allows for various functionalizations, which can enhance its pharmacological properties. Additionally, it may exhibit properties such as moderate to high melting points and stability under standard laboratory conditions. Its CAS number, 13877-56-0, is a unique identifier that facilitates its identification in chemical databases and literature. Overall, 1H-Pyrazolo[4,3-d]pyrimidin-7-amine is a compound of interest for further research in both synthetic and medicinal chemistry.
Formula:C5H5N5
InChI:InChI=1S/C5H5N5/c6-5-4-3(1-9-10-4)7-2-8-5/h1-2H,(H,9,10)(H2,6,7,8)
InChI key:InChIKey=MPDXYVOXVJOKIN-UHFFFAOYSA-N
SMILES:NC1=C2C(=NC=N1)C=NN2
Synonyms:- 1H-Pyrazolo[4,3-d]pyrimidine, 7-amino-
- 1H-pyrazolo[4,3-d]pyrimidin-7-amine
- 7-Aminopyrazolo(4,3-D)Pyrimidine
- NSC 81390
- Nsc81390
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Found 5 products.
1H-pyrazolo[4,3-d]pyrimidin-7-amine
CAS:Formula:C5H5N5Purity:97%Color and Shape:SolidMolecular weight:135.12671H-Pyrazolo[4,3-d]pyrimidin-7-amine
CAS:1H-Pyrazolo[4,3-d]pyrimidin-7-aminePurity:97%Molecular weight:135.13g/mol1H-Pyrazolo[4,3-d]pyrimidin-7-amine
CAS:Formula:C5H5N5Purity:95.0%Color and Shape:SolidMolecular weight:135.131H-Pyrazolo[4,3-d]pyrimidin-7-amine
CAS:<p>1H-Pyrazolo[4,3-d]pyrimidin-7-amine is a purine derivative that has been shown to have anti-leishmanial activity. It has been shown to be effective in the treatment of Leishmania donovani infections in mice without causing any adverse effects on the host. The previous studies show that 1H-pyrazolo[4,3-d]pyrimidin-7-amine inhibits the synthesis of purines, which are involved in nucleic acid and protein biosynthesis. This drug also appears to be more potent than other pyrazolopyrimidine derivatives because it targets ribonucleotide reductase. 1H-Pyrazolo[4,3-d]pyrimidin-7-amine is metabolized by cytochrome P450 enzymes and excreted as its metabolites in urine.</p>Formula:C5H5N5Purity:Min. 95%Molecular weight:135.13 g/mol



