Ethyl 2-amino-7-hydroxy-4-(pyridin-3-yl)-4H-chromene-3-carboxylate

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Ethyl 2-amino-7-hydroxy-4-(pyridin-3-yl)-4H-chromene-3-carboxylate manufacturers

  • HFI-142
  • HFI-142 pictures
  • $128.00
  • 2026-08-08
  • CAS:332164-34-8
  • Purity:
  • Supply Ability: 10g
Ethyl 2-amino-7-hydroxy-4-(pyridin-3-yl)-4H-chromene-3-carboxylate Basic information
Product Name:Ethyl 2-amino-7-hydroxy-4-(pyridin-3-yl)-4H-chromene-3-carboxylate
Synonyms:Ethyl 2-amino-7-hydroxy-4-(pyridin-3-yl)-4H-chromene-3-carboxylate;Ethyl 2-amino-7-hydroxy-4-(3-pyridinyl)-4H-1-benzopyran-3-carboxylate;HFI-142;4H-1-Benzopyran-3-carboxylic acid, 2-amino-7-hydroxy-4-(3-pyridinyl)-, ethyl ester;HFI 142,HFI142
CAS:332164-34-8
MF:C17H16N2O4
MW:312.32
EINECS:
Product Categories:
Mol File:332164-34-8.mol
Ethyl 2-amino-7-hydroxy-4-(pyridin-3-yl)-4H-chromene-3-carboxylate Structure
Ethyl 2-amino-7-hydroxy-4-(pyridin-3-yl)-4H-chromene-3-carboxylate Chemical Properties
Boiling point 513.0±50.0 °C(Predicted)
density 1.334±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
form Solid
pka9.18±0.70(Predicted)
color White to off-white
Safety Information
MSDS Information
Ethyl 2-amino-7-hydroxy-4-(pyridin-3-yl)-4H-chromene-3-carboxylate Usage And Synthesis
UsesEthyl 2-Amino-7-hydroxy-4-(pyridin-3-yl)-4H-chromene-3-carboxylate acts as a reagent in the synthesis, structural-activity relationship and the brain uptake of benzopyran inhibitors of insulin regulated aminopeptidase.
Ethyl 2-amino-7-hydroxy-4-(pyridin-3-yl)-4H-chromene-3-carboxylate Preparation Products And Raw materials
Tag:Ethyl 2-amino-7-hydroxy-4-(pyridin-3-yl)-4H-chromene-3-carboxylate(332164-34-8) Related Product Information
tert-butyl 2-amino-4-(pyridin-3-yl)-4H-benzo[h]chromene-3-carboxylate Ethyl 2-amino-7-hydroxy-4-(pyridin-3-yl)-4H-chromene-3-carboxylate HFI-437 ethyl 2-amino-4-(1-cyano-2-ethoxy-2-oxoethyl)-4H-chromene-3-carboxylate ethyl 2-amino-4-(pyridin-3-yl)-4H-benzo[h]chromene-3-carboxylate ethyl 2-amino-4-(cyano-ethoxycarbonyl-methyl)-4H-chromene-3-carboxylate