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CAS 1239460-82-2

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5,6-Dibromothieno[2,3-d]pyrimidin-4(1H)-one

Description:
5,6-Dibromothieno[2,3-d]pyrimidin-4(1H)-one is a heterocyclic compound characterized by its fused thieno and pyrimidine rings, which contribute to its unique chemical properties. The presence of two bromine atoms at the 5 and 6 positions enhances its reactivity and can influence its biological activity. This compound typically exhibits a solid state at room temperature and is soluble in organic solvents, reflecting its non-polar characteristics. The thienopyrimidine structure is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its ability to interact with biological targets. The compound may also display interesting electronic properties owing to the conjugated system formed by the aromatic rings. Its synthesis and characterization are of interest in research, particularly in the fields of drug discovery and materials science. As with many brominated compounds, it is essential to handle it with care due to potential environmental and health impacts associated with halogenated organic compounds.
Formula:C6H2Br2N2OS
InChI:InChI=1S/C6H2Br2N2OS/c7-3-2-5(11)9-1-10-6(2)12-4(3)8/h1H,(H,9,10,11)
InChI key:InChIKey=VPUOHESABWTXNI-UHFFFAOYSA-N
SMILES:BrC=1C2=C(SC1Br)NC=NC2=O
Synonyms:
  • 5,6-Dibromothieno[2,3-d]pyrimidin-4(1H)-one
  • Thieno[2,3-d]pyrimidin-4(1H)-one, 5,6-dibromo-
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