CAS 20555-88-8
:6-(hydroxyamino)pyrimidin-2(1H)-one
Description:
6-(Hydroxyamino)pyrimidin-2(1H)-one, with the CAS number 20555-88-8, is an organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. This compound features a hydroxyamino group (-NH2OH) at the 6-position and a carbonyl group (C=O) at the 2-position, contributing to its reactivity and potential biological activity. It is typically a white to off-white solid and is soluble in polar solvents due to the presence of the hydroxyl and amino functional groups. The compound may exhibit properties such as being a potential intermediate in the synthesis of pharmaceuticals or agrochemicals, and it may also participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. Its biological significance may be linked to its role in nucleic acid metabolism or as a building block in the synthesis of nucleobases. As with many nitrogen-containing heterocycles, it may also display interesting pharmacological properties.
Formula:C4H5N3O2
InChI:InChI=1/C4H5N3O2/c8-4-5-2-1-3(6-4)7-9/h1-2,9H,(H2,5,6,7,8)
SMILES:c1cnc(nc1NO)O
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Found 9 products.
2(1H)-Pyrimidinone, 6-(hydroxyamino)-
CAS:Formula:C4H5N3O3Purity:97%Color and Shape:SolidMolecular weight:143.10086-HYDROXYLAMINOURACIL
CAS:6-HYDROXYLAMINOURACIL is a derivative of uracil, which induces DNA damage and apoptosis in tumor cells and inhibits tumor cell growth in vitro.Formula:C4H5N3O2Purity:99.98%Color and Shape:SolidMolecular weight:127.1Ref: TM-T9463
1mg64.00€5mg131.00€10mg188.00€25mg299.00€50mg427.00€100mg575.00€200mg750.00€1mL*10mM (DMSO)94.00€N4-Hydroxycytosine
CAS:N4-Hydroxycytosine is an intramolecular hydrogen that inhibits the replication of viruses by inhibiting their DNA polymerase. It is a structural analogue of cytosine and can be found in both left- and right-handed forms, which are termed isomers. The chemical study of N4-hydroxycytosine has shown it to have inhibitory effects on human immunodeficiency virus and hepatitis C virus. 13C-NMR spectroscopy has been used to identify the chemical structure of N4-hydroxycytosine and its reactivity with other molecules. N4-Hydroxycytosine can be synthesized by the reaction between formaldehyde and 2,3,5,6-tetrafluorocytosine.Formula:C4H5N3O2Purity:Min. 95%Color and Shape:PowderMolecular weight:127.1 g/molN4-Hydroxycytosine (>90%)
CAS:Controlled ProductFormula:C4H5N3O2Purity:>90%Color and Shape:NeatMolecular weight:127.1






