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CAS 458543-81-2

:

Ethyl 3-amino-2,6-dichloro-4-pyridinecarboxylate

Description:
Ethyl 3-amino-2,6-dichloro-4-pyridinecarboxylate is an organic compound characterized by its pyridine ring structure, which is substituted at specific positions with amino and dichloro groups, as well as an ethyl ester functional group. This compound typically exhibits properties associated with both amines and esters, such as potential solubility in polar solvents and the ability to participate in various chemical reactions, including nucleophilic substitutions and acylation. The presence of chlorine atoms enhances its reactivity and may influence its biological activity, making it of interest in medicinal chemistry. The amino group can act as a hydrogen bond donor, while the carboxylate moiety can engage in hydrogen bonding and ionic interactions. Ethyl 3-amino-2,6-dichloro-4-pyridinecarboxylate may be utilized in the synthesis of pharmaceuticals or agrochemicals, given its structural features that can be tailored for specific biological activities. Safety and handling precautions should be observed due to the potential toxicity associated with chlorinated compounds.
Formula:C8H8Cl2N2O2
InChI:InChI=1/C8H8Cl2N2O2/c1-2-14-8(13)4-3-5(9)12-7(10)6(4)11/h3H,2,11H2,1H3
InChI key:InChIKey=ZBHSEGWPJCOBKP-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C=1C(N)=C(Cl)N=C(Cl)C1
Synonyms:
  • Ethyl 3-amino-2,6-dichloro-4-pyridinecarboxylate
  • 4-Pyridinecarboxylic acid, 3-amino-2,6-dichloro-, ethyl ester
  • 3-Amino-2,6-dichloro-isonicotinic acid ethyl ester
  • 3-AMINO-2,6-DICHLOROPYRIDINE-4-CARBOXYLIC ACID METHYL ESTER
  • Methyl 3-amino-2,6-dichloro-4-pyridinecarboxylate
  • METHYL 3-AMINO-2,6-DICHLOROISONICOTINATE
  • Ethyl 3-amino-2,6-dichloropyridine-4-carboxylate
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