CAS 1312535-79-7
:2-Chloro-α-methyl-4-pyrimidinemethanol
Description:
2-Chloro-α-methyl-4-pyrimidinemethanol is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic heterocycle containing nitrogen atoms. The presence of a chlorine atom at the second position and a hydroxymethyl group at the fourth position contributes to its unique reactivity and potential applications in medicinal chemistry. This compound typically exhibits moderate solubility in polar solvents due to the hydroxyl group, while the chlorine substituent may influence its lipophilicity and biological activity. The α-methyl group enhances steric hindrance, which can affect the compound's interaction with biological targets. As a pyrimidine derivative, it may exhibit properties relevant to nucleic acid metabolism or enzyme inhibition, making it of interest in pharmaceutical research. Safety data and handling precautions should be considered, as with any chemical substance, to ensure proper laboratory practices. Overall, 2-Chloro-α-methyl-4-pyrimidinemethanol represents a class of compounds that can be explored for various chemical and biological applications.
Formula:C6H7ClN2O
InChI:InChI=1S/C6H7ClN2O/c1-4(10)5-2-3-8-6(7)9-5/h2-4,10H,1H3
InChI key:InChIKey=MIUDYNZFUBDJPT-UHFFFAOYSA-N
SMILES:C(C)(O)C1=NC(Cl)=NC=C1
Synonyms:- 1-(2-Chloropyrimidin-4-yl)ethan-1-ol
- 4-Pyrimidinemethanol, 2-chloro-α-methyl-
- 2-Chloro-α-methyl-4-pyrimidinemethanol
- 1-(2-Chloropyrimidin-4-yl)ethanol
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