CAS 1263283-21-1

4,6-Dichloro-2-cyclopropyl-5-pyrimidinemethanol

Description:

4,6-Dichloro-2-cyclopropyl-5-pyrimidinemethanol is a chemical compound characterized by its pyrimidine ring structure, which is substituted at the 4 and 6 positions with chlorine atoms, and at the 2 position with a cyclopropyl group. The presence of the hydroxymethyl group at the 5 position contributes to its reactivity and potential biological activity. This compound is typically classified as a heterocyclic organic compound, and its molecular structure suggests it may exhibit properties relevant to medicinal chemistry, particularly in the development of pharmaceuticals. The dichloro substitutions can enhance its lipophilicity and influence its interaction with biological targets. Additionally, the cyclopropyl group may impart unique steric and electronic properties, potentially affecting the compound's pharmacokinetics and pharmacodynamics. As with many pyrimidine derivatives, it may be of interest in the study of nucleic acid metabolism or as a scaffold for drug design. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

Formula: C₈H₈Cl₂N₂O

InChI: InChI=1S/C8H8Cl2N2O/c9-6-5(3-13)7(10)12-8(11-6)4-1-2-4/h4,13H,1-3H2

InChI key: InChIKey=XVMOVSKQAQZKQT-UHFFFAOYSA-N

SMILES: ClC1=NC(=NC(Cl)=C1CO)C2CC2

Synonyms:

• 5-Pyrimidinemethanol, 4,6-dichloro-2-cyclopropyl-
• 4,6-Dichloro-2-cyclopropyl-5-pyrimidinemethanol