CAS 1979-98-2
:4,6-dihydroxy-2-methylmercaptopyrimidine
Description:
4,6-Dihydroxy-2-methylmercaptopyrimidine, with the CAS number 1979-98-2, is a heterocyclic organic compound that features a pyrimidine ring substituted with hydroxyl and thiol groups. This compound is characterized by the presence of two hydroxyl (-OH) groups at the 4 and 6 positions and a methylthio (-SCH3) group at the 2 position of the pyrimidine ring. These functional groups contribute to its chemical reactivity and potential biological activity. The hydroxyl groups can participate in hydrogen bonding, enhancing solubility in polar solvents, while the thiol group can engage in redox reactions and form disulfide bonds. This compound may exhibit antioxidant properties and could be of interest in pharmaceutical applications, particularly in the development of drugs targeting various biological pathways. Its structural features suggest potential interactions with enzymes or receptors, making it a candidate for further research in medicinal chemistry. Overall, 4,6-dihydroxy-2-methylmercaptopyrimidine is a versatile compound with significant implications in both synthetic and biological chemistry.
Formula:C5H6N2O2S
InChI:InChI=1/C5H6N2O2S/c1-10-5-6-3(8)2-4(9)7-5/h2H2,1H3,(H,6,7,8,9)
InChI key:InChIKey=AEXCUJUYEZIWJV-UHFFFAOYSA-N
SMILES:S(C)C=1NC(=O)C=C(O)N1
Synonyms:- 2-(Methylthio)-4,6-dihydroxypyrimidine
- 2-(methylsulfanyl)pyrimidine-4,6(1H,5H)-dione
- 2-Methylmercapto-4,6-dihydroxypyrimidine
- 2-Methylsulfanylpyrimidine-4,6-diol
- 2-Methylthio-4,6-pyrimidinedione
- 2-Methylthiopyrimidine-4,6-diol
- 4(1H)-Pyrimidinone, 6-hydroxy-2-(methylthio)-
- 4(3H)-Pyrimidinone, 6-hydroxy-2-(methylthio)-
- 4,6-Dihydroxy-2-(methylmercapto)pyrimidine
- 4,6-Dihydroxy-2-methylthio pyrimidine
- 4,6-Dihydroxy-2-methythiopyrimidine
- 4,6-Pyrimidinediol, 2-(methylthio)-
- 6-Hydroxy-2-(methylthio)-4(1H)-pyrimidinone
- 6-Hydroxy-2-(methylthio)-4(3H)-pyrimidinone
- 6-Hydroxy-2-(methylthio)-4-pyrimidinone
- 6-hydroxy-2-(methylsulfanyl)pyrimidin-4(3H)-one
- NSC 44557
- S-Methylthiobarbituric acid
- 2-Methylthiopyrimidin-4,6-diol
- 2-(Methylmercapto)-4,6-pyrimidinediol
- 2-Mercapto thobarbituric acid
- 2-METHYLTHIO-4,6-PYRIMIDINEDIOL
- 2-Methylthiobarbituric acid
- 2-Thiomethyl 4,6-Dihydroxy Pyrimidine
- 2-(Methylmercapto)-4,6-Pyrimid
- DIHYDROXY-2-METHYLMERCAPTOPYRIMIDINE
- S-MTBA
- 4,6-DIHYDROXY-2-METHYLMERCAPTOPYRIMIDINE
- 4,6-dihydroxy-2-methylmercaprimidine
- 4,6-dihydroxyl-2-methylthio-pyrimidine
- 2-methylthio-4,6-dihydroxylpyrimidine
- See more synonyms
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Found 7 products.
S-Methylthiobarbituric Acid
CAS:Formula:C5H6N2O2SPurity:>98.0%(T)(HPLC)Color and Shape:White to Light yellow to Dark green powder to crystalMolecular weight:158.184(3H)-Pyrimidinone, 6-hydroxy-2-(methylthio)-
CAS:Formula:C5H6N2O2SPurity:95%Color and Shape:SolidMolecular weight:158.17836-Hydroxy-2-(methylthio)pyrimidin-4(3H)-one
CAS:<p>6-Hydroxy-2-(methylthio)pyrimidin-4(3H)-one</p>Formula:C5H6N2O2SPurity:98%Color and Shape: white solidMolecular weight:158.17834g/mol4,6-Dihydroxy-2-methylmercaptopyrimidine
CAS:Formula:C5H6N2O2SPurity:95%Color and Shape:Solid, Off white powderMolecular weight:158.182-Methylthio-4,6-dihydroxypyrimidine
CAS:<p>2-Methylthio-4,6-dihydroxypyrimidine is an organic compound that has a hypsochromic and bathochromic effect. This ligand belongs to the group of neutral compounds and is found in its intramolecular hydrogen form. It also reacts with hydrochloric acid to form tautomers. 2-Methylthio-4,6-dihydroxypyrimidine can exist in two tautomeric forms: the chloride and oxalyl forms. The vibrational frequencies of these tautomers are different. 2-Methylthio-4,6-dihydroxypyrimidine is an intermediate in the synthesis of other chemical compounds such as chloropropionates, methanesulfonic acid, and piperazine.</p>Formula:C5H6N2O2SPurity:Min. 95%Color and Shape:PowderMolecular weight:158.18 g/mol2-(Methylthio)-4,6-pyrimidinediol
CAS:Controlled ProductFormula:C5H6N2O2SColor and Shape:NeatMolecular weight:158.18






