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CAS 14160-93-1

:

4-Amino-6-chloropyrimidine-5-carbaldehyde

Description:
4-Amino-6-chloropyrimidine-5-carbaldehyde is a heterocyclic organic compound characterized by its pyrimidine ring structure, which includes an amino group and a chlorinated position. The presence of the aldehyde functional group at the 5-position contributes to its reactivity, making it useful in various chemical syntheses. This compound typically appears as a solid and is soluble in polar solvents, reflecting its functional groups' ability to engage in hydrogen bonding. It is often utilized in pharmaceutical chemistry and the synthesis of biologically active molecules due to its potential as an intermediate in the development of drugs. The compound's reactivity can be attributed to the electron-withdrawing effects of the chlorine atom and the aldehyde group, which can influence its behavior in nucleophilic reactions. Safety data indicates that, like many nitrogen-containing heterocycles, it should be handled with care, as it may pose health risks if ingested or inhaled. Overall, 4-Amino-6-chloropyrimidine-5-carbaldehyde is a valuable compound in organic synthesis and medicinal chemistry.
Formula:C5H4ClN3O
InChI:InChI=1/C5H4ClN3O/c6-4-3(1-10)5(7)9-2-8-4/h1-2H,(H2,7,8,9)
InChI key:InChIKey=GOJNFUXEBVBARW-UHFFFAOYSA-N
SMILES:C(=O)C=1C(Cl)=NC=NC1N
Synonyms:
  • 4-Amino-6-chloro-5-pyrimidine carbaldehyde
  • 4-Amino-6-chloro-5-pyrimidinecarboxaldehyde
  • 4-Amino-6-chloro-pyrimidine-5-carbaldehyde
  • 4-Amino-6-chloropyrimidine-5-carboxaldehyde
  • 5-Pyrimidinecarboxaldehyde, 4-amino-6-chloro-
  • 6-Chloro-5-difluoromethyl-pyrimidin-4-ylamine
  • 4-Amino-6-chloropyrimidine-5-carbaldehyde
  • 4-Chloro-6-aminopyrimidine-5-carbaldehyde
  • 4-Amino-6-chloro-5-formylpyrimidine, 4-Amino-6-chloro-5-formyl-1,3-diazine
  • 4-Amino-6-chloropyrimidine-5-carboxaldehyde,97%
  • See more synonyms
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