CAS 43005-49-8
:6-amino-2-(methylsulfanyl)-5-nitrosopyrimidin-4(1H)-one
Description:
6-Amino-2-(methylsulfanyl)-5-nitrosopyrimidin-4(1H)-one, with the CAS number 43005-49-8, is a heterocyclic organic compound that features a pyrimidine ring, which is a six-membered aromatic ring containing two nitrogen atoms. This compound is characterized by the presence of an amino group (-NH2), a nitroso group (-NO), and a methylthio group (-S-CH3) attached to the pyrimidine structure. The nitroso group contributes to its potential reactivity and biological activity, while the methylthio group may influence its solubility and interaction with other molecules. The compound's structure suggests it may participate in various chemical reactions, including nucleophilic substitutions and redox reactions. Its unique functional groups may also impart specific pharmacological properties, making it of interest in medicinal chemistry. Additionally, the compound's stability, solubility, and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations for its practical applications.
Formula:C5H6N4O2S
InChI:InChI=1/C5H6N4O2S/c1-12-5-7-3(6)2(9-11)4(10)8-5/h1H3,(H3,6,7,8,10)
SMILES:CSc1nc(c(c(n1)O)N=O)N
Synonyms:- 4(3H)-pyrimidinone, 6-amino-2-(methylthio)-5-nitroso-
- 6-Amino-2-(methylsulfanyl)-5-nitrosopyrimidin-4(3H)-one
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Found 2 products.
6-Amino-2-(methylthio)-5-nitrosopyrimidin-4(3H)-one
CAS:<p>6-Amino-2-(methylthio)-5-nitrosopyrimidin-4(3H)-one</p>Purity:95%Molecular weight:186.2g/mol6-Amino-2-(methylsulfanyl)-5-nitroso-3,4-dihydropyrimidin-4-one
CAS:<p>6-Amino-2-(methylsulfanyl)-5-nitroso-3,4-dihydropyrimidin-4-one is a metal complex that has been shown to dehalogenate chloroform and bromotrichloromethane. The enthalpy change for this reaction was measured by calorimetry and found to be -14.8 kJ/mol. This complex also undergoes dehydration with the release of water, which was confirmed by thermal analysis.</p>Formula:C5H6N4O2SPurity:Min. 95%Molecular weight:186.19 g/mol


