CAS 5915-16-2
:[1,2,4]triazolo[1,5-a]pyrimidin-7-amine
Description:
[1,2,4]Triazolo[1,5-a]pyrimidin-7-amine is a heterocyclic compound characterized by its fused triazole and pyrimidine rings, which contribute to its unique chemical properties. This compound typically exhibits a solid-state structure and is known for its potential biological activity, making it of interest in medicinal chemistry. The presence of the amino group at the 7-position enhances its reactivity and solubility in polar solvents. It may participate in hydrogen bonding due to the amino group, influencing its interactions with biological targets. The compound's structure allows for various substitutions, which can modify its pharmacological properties. Additionally, [1,2,4]triazolo[1,5-a]pyrimidin-7-amine may exhibit properties such as moderate to high melting points and stability under standard laboratory conditions. Its applications can range from pharmaceuticals to agrochemicals, depending on the specific derivatives and modifications made to the core structure. Overall, this compound represents a versatile scaffold in the development of new therapeutic agents.
Formula:C5H5N5
InChI:InChI=1/C5H5N5/c6-4-1-2-7-5-8-3-9-10(4)5/h1-3H,6H2
SMILES:c1cnc2ncnn2c1N
Synonyms:- [1,2,4]Triazolo[1,5-a]pyrimidin-7-amine
- [1,2,4]triazolo[1,5-a]pyrimidin-7-ylamine
- [1,2,4]triazolo[5,1-b]pyrimidin-7-ylamine
- [1,2,4]triazolo[5,1-b]pyrimidin-7-amine
- 1,5,7,9-tetrazabicyclo[4.3.0]nona-2,4,6,8-tetraen-2-amine
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Found 4 products.
[1,2,4]Triazolo[1,5-a]pyriMidin-7-aMine
CAS:Formula:C5H5N5Purity:97%Color and Shape:SolidMolecular weight:135.1267[1,2,4]Triazolo[1,5-a]pyrimidin-7-amine
CAS:[1,2,4]Triazolo[1,5-a]pyrimidin-7-aminePurity:95%Molecular weight:135.13g/mol[1,2,4]Triazolo[1,5-a]pyrimidin-7-amine
CAS:Formula:C5H5N5Purity:97%Color and Shape:SolidMolecular weight:135.13[1,2,4]Triazolo[1,5-a]pyrimidin-7-amine
CAS:<p>[1,2,4]Triazolo[1,5-a]pyrimidin-7-amine is a competitive inhibitor of tumor growth. It has been shown to inhibit the synthesis of DNA and RNA by binding to the N7 nitrogen atom in the nucleotide base. The compound also has a trifluoromethyl group that can be used as an assay for enzymatic activity. [1,2,4]Triazolo[1,5-a]pyrimidin-7-amine can be synthesized from 2-(3'-hydroxypropoxy)phenylamine by reaction with hydroxylamine and formaldehyde in the presence of sodium cyanide. This drug inhibits tumor growth in vitro and in vivo and is active against infectious diseases such as hepatitis B virus (HBV).</p>Formula:C5H5N5Purity:Min. 95%Molecular weight:135.13 g/mol




