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CAS 62501-45-5

:

2(1H)-Pyrimidinethione, 4,6-dimethyl-, hydrochloride (1:1)

Description:
2(1H)-Pyrimidinethione, 4,6-dimethyl-, hydrochloride (1:1) is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic heterocycle containing two nitrogen atoms at positions 1 and 3. This compound features a thione functional group, indicating the presence of a sulfur atom double-bonded to a carbon atom, which contributes to its reactivity and potential biological activity. The presence of methyl groups at the 4 and 6 positions of the pyrimidine ring enhances its lipophilicity and may influence its interaction with biological targets. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, which is advantageous for pharmaceutical applications. The compound may exhibit various pharmacological properties, making it of interest in medicinal chemistry. Its CAS number, 62501-45-5, allows for easy identification and reference in chemical databases. Overall, this compound's unique structural features and properties make it a subject of interest in both research and potential therapeutic applications.
Formula:C6H8N2S·ClH
InChI:InChI=1S/C6H8N2S.ClH/c1-4-3-5(2)8-6(9)7-4;/h3H,1-2H3,(H,7,8,9);1H
InChI key:InChIKey=KAHPDWLNROMIHC-UHFFFAOYSA-N
SMILES:CC1=CC(C)=NC(=S)N1.Cl
Synonyms:
  • 2(1H)-Pyrimidinethione, 4,6-dimethyl-, hydrochloride (1:1)
  • 2(1H)-Pyrimidinethione, 4,6-dimethyl-, monohydrochloride
  • 2-Mercapto-4,6-dimethylpyrimidin-1-ium chloride
  • 2-Mercapto-4,6-dimethylpyrimidine hydrochloride
  • 4,6-Dimethyl-1H-pyrimidine-2-thione monohydrochloride
  • 4,6-Dimethyl-2-mercaptopyrimidine hydrochloride
  • 4,6-Dimethyl-2-pyrimidinethiol hydrochloride
  • 4,6-Dimethylpyrimidine-2(1H)-thione monohydrochloride
  • 4,6-dimethylpyrimidine-2(1H)-thione hydrochloride
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