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CAS 68462-61-3

:

Ethyl 5-amino-1-(phenylmethyl)-1H-imidazole-4-carboxylate

Description:
Ethyl 5-amino-1-(phenylmethyl)-1H-imidazole-4-carboxylate is a chemical compound characterized by its imidazole ring, which is a five-membered aromatic heterocycle containing two nitrogen atoms. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of an amino group at the 5-position of the imidazole ring enhances its potential for biological activity, making it of interest in medicinal chemistry. The phenylmethyl group (benzyl) at the 1-position provides additional steric and electronic properties that can influence the compound's interactions with biological targets. Ethyl 5-amino-1-(phenylmethyl)-1H-imidazole-4-carboxylate may exhibit various properties such as moderate to high polarity, depending on the functional groups present, and it may participate in hydrogen bonding due to the amino and carboxylate functionalities. Its CAS number, 68462-61-3, allows for easy identification in chemical databases, facilitating research and application in various fields, including pharmaceuticals and agrochemicals.
Formula:C13H15N3O2
InChI:InChI=1/C13H15N3O2/c1-2-18-13(17)11-12(14)16(9-15-11)8-10-6-4-3-5-7-10/h3-7,9H,2,8,14H2,1H3
InChI key:InChIKey=CJCXZTWYOFENDL-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C1=C(N)N(CC2=CC=CC=C2)C=N1
Synonyms:
  • 1H-Imidazole-4-carboxylic acid, 5-amino-1-(phenylmethyl)-, ethyl ester
  • 5-Amino-1-benzyl-1H-imidazole-4-carboxylic acid ethyl ester
  • Ethyl 5-amino-1-(phenylmethyl)-1H-imidazole-4-carboxylate
  • Ethyl 5-amino-1-benzyl-1H-imidazole-4-carboxylate
  • Ethyl 5-amino-1-benzyl-1H-imidazole-4-carboxylate 95+%
  • 5-amino-1-benzylimidazole-4-carboxylate
  • ETHYL 5-AMINO-1-BENZYLIMIDAZOLE-4-CARBOXYLATE
  • AKOS BB-9609
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