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CAS 16462-26-3

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4-Amino-2-mercaptopyrimidine-5-carbonitrile

Description:
4-Amino-2-mercaptopyrimidine-5-carbonitrile is a heterocyclic organic compound characterized by its pyrimidine ring structure, which contains both amino and mercapto functional groups. The presence of the amino group (-NH2) contributes to its basicity and potential for forming hydrogen bonds, while the mercapto group (-SH) imparts thiol characteristics, making it reactive in various chemical reactions. The carbonitrile group (-C≡N) enhances the compound's polarity and can participate in nucleophilic addition reactions. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to its functional groups. Its unique structure suggests potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. Additionally, the compound may exhibit biological activity, which warrants further investigation for potential therapeutic uses. Safety data should be consulted, as compounds containing thiol and amino groups can be sensitive to oxidation and may pose health risks if not handled properly.
Formula:C5H4N4S
InChI:InChI=1/C5H4N4S/c6-1-3-2-8-5(10)9-4(3)7/h2H,(H3,7,8,9,10)
SMILES:C(#N)c1c[nH]c(nc1=N)S
Synonyms:
  • 4-Amino-2-sulfanyl-5-pyrimidinecarbonitrile
  • 6-Amino-2-Thioxo-1,2-Dihydropyrimidine-5-Carbonitrile
  • 4-Amino-2-mercaptopyrimidine-5-carbonitrile ,97%
  • 6-amino-2-sufanylidene-1H-pyrimidine-5-carbonitrile
  • 4-AMINO-2-MERCAPTOPYRIMIDINE-5-CARBONITRILE ISO 9001:2015 REACH
  • 6-Amino-1,2-dihydro-2-thioxo-5-pyrimidinecarbonitrile
  • 4-Amino-2-mercaptopyrimidine-5-carbonitrile
  • 6-amino-2-sulfanylidene-1H-pyrimidine-5-carbonitrile
  • 5-PyriMidinecarbonitrile, 6-aMino-1,2-dihydro-2-thioxo-
  • 4-AMino-2-sulfanylpyriMidine-5-carbonitrile
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