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CAS 215927-36-9

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6-bromothieno[3,2-d]pyrimidin-4(3H)-one

Description:
6-Bromothieno[3,2-d]pyrimidin-4(3H)-one is a heterocyclic organic compound characterized by its unique fused ring structure, which combines a thieno and pyrimidinone moiety. The presence of a bromine atom at the 6-position contributes to its reactivity and potential applications in medicinal chemistry. This compound typically exhibits properties such as moderate solubility in organic solvents and stability under standard laboratory conditions. Its molecular structure suggests potential for interactions with biological targets, making it of interest in drug discovery and development. The thieno and pyrimidinone rings can participate in various chemical reactions, including nucleophilic substitutions and cycloadditions, which may be exploited for synthesizing derivatives with enhanced biological activity. Additionally, the compound's unique electronic properties, influenced by the bromine substituent, may affect its pharmacokinetic and pharmacodynamic profiles. Overall, 6-bromothieno[3,2-d]pyrimidin-4(3H)-one represents a valuable scaffold for further research in the field of organic and medicinal chemistry.
Formula:C6H3BrN2OS
InChI:InChI=1/C6H3BrN2OS/c7-4-1-3-5(11-4)6(10)9-2-8-3/h1-2H,(H,8,9,10)
InChI key:IJSCGMBLRLDHPZ-UHFFFAOYSA-N
SMILES:c1c2c(c(=O)[nH]cn2)sc1Br
Synonyms:
  • 6-Bromothieno[3,2-d]pyrimidin-4(1H)-one
  • Thieno[3,2-d]pyrimidin-4(1H)-one, 6-bromo-
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