CAS 28466-26-4
:1H-Pyrazol-4-amine
Description:
1H-Pyrazol-4-amine, with the CAS number 28466-26-4, is an organic compound characterized by its pyrazole ring structure, which consists of a five-membered ring containing two nitrogen atoms at adjacent positions. This compound features an amino group (-NH2) attached to the fourth carbon of the pyrazole ring, contributing to its reactivity and potential applications in various fields. It is typically a white to off-white solid, and its solubility can vary depending on the solvent used. 1H-Pyrazol-4-amine is of interest in medicinal chemistry and material science due to its potential as a building block for pharmaceuticals and agrochemicals. The presence of the amino group allows for further functionalization, making it versatile in synthetic chemistry. Additionally, it may exhibit biological activity, which warrants investigation for its potential therapeutic applications. As with many nitrogen-containing heterocycles, it may also participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Proper handling and safety measures should be observed due to its chemical properties.
Formula:C3H5N3
InChI:InChI=1S/C3H5N3/c4-3-1-5-6-2-3/h1-2H,4H2,(H,5,6)
InChI key:InChIKey=AXINVSXSGNSVLV-UHFFFAOYSA-N
SMILES:NC=1C=NNC1
Synonyms:- 1H-Pyrazol-4-Ylamine
- 1H-pyrazol-4-amine
- 4-Aminopyrazole
- Pyrazole, 4-amino-
- 4-Amino-1H-pyrazole
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Found 6 products.
1H-Pyrazol-4-amine
CAS:Formula:C3H5N3Purity:>98.0%(GC)(T)Color and Shape:White to Brown to Dark purple powder to crystalMolecular weight:83.094-Amino-1H-pyrazole
CAS:4-Amino-1H-pyrazoleFormula:C3H5N3Purity:≥95%Color and Shape:Brown SolidMolecular weight:83.09194-Amino-1H-pyrazole
CAS:4-Amino-1H-pyrazole is a synthetic compound that inhibits the coagulation pathway by inhibiting the synthesis of prothrombin and factor VII. This compound has been shown to be effective in treating autoimmune diseases and cancer. 4-Amino-1H-pyrazole binds to a unique site on the coagulation enzyme, which is not present in other thrombin inhibitors, such as hirudin and heparin. The binding site overlaps with the kinase domain, which inhibits protein synthesis by preventing phosphorylation of key enzymes. In addition, it inhibits wild type strains of bacteria and has been shown to inhibit the growth of cancer cells.
Formula:C3H5N3Purity:Min. 95%Molecular weight:83.09 g/molRef: 10-F043675
Discontinued product
