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CAS 54503-94-5

:

4-Chloro-6-(4-morpholinyl)-5-pyrimidinecarboxaldehyde

Description:
4-Chloro-6-(4-morpholinyl)-5-pyrimidinecarboxaldehyde is a chemical compound characterized by its pyrimidine ring structure, which is substituted with a chloro group and a morpholine moiety. The presence of the aldehyde functional group contributes to its reactivity, making it useful in various synthetic applications. This compound typically appears as a solid or crystalline substance and is soluble in polar organic solvents. Its molecular structure suggests potential biological activity, which has led to interest in its use in medicinal chemistry, particularly in the development of pharmaceuticals. The morpholine group may enhance the compound's ability to interact with biological targets, potentially influencing its pharmacokinetic properties. As with many chemical substances, safety precautions should be observed when handling it, as it may pose health risks. Overall, 4-Chloro-6-(4-morpholinyl)-5-pyrimidinecarboxaldehyde is notable for its unique structural features and potential applications in research and industry.
Formula:C9H10ClN3O2
InChI:InChI=1S/C9H10ClN3O2/c10-8-7(5-14)9(12-6-11-8)13-1-3-15-4-2-13/h5-6H,1-4H2
InChI key:InChIKey=YGFLPSPKKFXHHX-UHFFFAOYSA-N
SMILES:C(=O)C=1C(=NC=NC1Cl)N2CCOCC2
Synonyms:
  • 4-Chloro-6-(4-morpholinyl)-5-pyrimidinecarboxaldehyde,
  • 4-Chloro-6-(morpholin-4-yl)pyrimidine-5-carboxaldehyde
  • 4-Chloro-6-morpholin-4-ylpyrimidine-5-carboxaldehyde
  • 4-Chloro-6-morpholino-5-pyrimidinecarbaldehyde
  • 4-Morpholino-6-chloro-5-formylpyrimidine
  • 5-Pyrimidinecarboxaldehyde, 4-chloro-6-(4-morpholinyl)-
  • 54503-94-5
  • T6N Dotj A- Dt6N Cnj Evh Fg
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