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CAS 20419-68-5

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2,6-Dichloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine

Description:
2,6-Dichloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine is a purine derivative characterized by the presence of two chlorine atoms at the 2 and 6 positions of the purine ring, which contributes to its unique chemical properties. The compound features a tetrahydro-2H-pyran moiety attached at the 9-position, which enhances its solubility and biological activity. This structure suggests potential interactions with biological targets, making it of interest in medicinal chemistry. The presence of chlorine atoms typically influences the compound's reactivity and stability, while the tetrahydropyran group may affect its pharmacokinetic properties, such as absorption and metabolism. The compound is likely to exhibit moderate to high lipophilicity due to the hydrophobic nature of the purine ring and the tetrahydropyran substituent. Additionally, its molecular structure may allow for hydrogen bonding and other interactions with biological macromolecules, which is crucial for its potential applications in drug development. Overall, 2,6-Dichloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine represents a complex chemical entity with promising characteristics for further research.
Formula:C10H10Cl2N4O
InChI:InChI=1/C10H10Cl2N4O/c11-8-7-9(15-10(12)14-8)16(5-13-7)6-3-1-2-4-17-6/h5-6H,1-4H2
InChI key:InChIKey=ASNBMEFTEPQHDX-UHFFFAOYSA-N
SMILES:ClC1=C2C(N(C=N2)C3CCCCO3)=NC(Cl)=N1
Synonyms:
  • 2,6-Dichloro-9-(oxan-2-yl)purine
  • 2,6-Dichloro-9-(tetrahydro-2H-pyran-2-yl)purine
  • 2,6-Dichloro-9-(tetrahydropyran-2-yl)-9H-purine
  • 9-(Tetrahydropyran-2-yl)-2,6-dichloro-9H-purine
  • 9H-purine, 2,6-dichloro-9-(tetrahydro-2H-pyran-2-yl)-
  • NSC 112526
  • 2,6-Dichloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine
  • 2,6-dichloro-9-(oxan-2-yl)-9H-purine
  • 2,6-dichloro-9-tetrahydropyran-2-yl-purine
  • 2,6-Dichloro-9-(2-tetrahydropyranyl)-9H-purine
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