23789-87-9

Basic information

• Product Name: 3-Quinolinecarboxylicacid, 1-ethyl-1,4-dihydro-4-oxo-, ethyl ester
• Synonyms: H 4380
• CAS NO: 23789-87-9
• Molecular Formula: C14H15 N O3
• Molecular Weight: 245.278
• Mol File: 23789-87-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 3-Quinolinecarboxylicacid, 1-ethyl-1,4-dihydro-4-oxo-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Quinolinecarboxylicacid, 1-ethyl-1,4-dihydro-4-oxo-, ethyl ester(23789-87-9)
• EPA Substance Registry System: 3-Quinolinecarboxylicacid, 1-ethyl-1,4-dihydro-4-oxo-, ethyl ester(23789-87-9)

Safety Data

• Hazardous Substances Data: 23789-87-9(Hazardous Substances Data)

Upstream product

• 74-96-4 ethyl bromide 
• 52980-28-6 ethyl 4-oxo-1,4-dihydroquinoline-3-carboxylate 
• 75-03-6 ethyl iodide 
• 78-40-0 triethyl phosphate 

Downstream Products

• 1456629-62-1 1-ethyl-4-oxo-1,4-dihydro-3-[1-oxo-2-hydrazino-3-{p-toluenesulfon}]quinoline 

Relevant articles and documents

BORON CONTAINING COMPOUNDS AND THEIR USES

The present disclosure contemplates a boron-containing compound, a composition containing a pesticidal effective amount of that compound dissolved or dispersed in a carrier medium, and a method of reducing, ameliorating, or controlling an infestation by a pest, particularly a fungus, by administering a contemplated composition to a plant or animal in need.

Synthesis and study of 1-ethyl-3-carbohydrazide and 3-[1-oxo-2-hydrazino-3- {p-toluenesulfon}]quinolone derivatives against bacterial infections

We have synthesized newer series of quinolone derivatives substituted with hydrazine group (6a-e) and sulfonamide group (7a-e). These compounds were screened for antibacterial activity. All these compounds were fully characterized by spectroscopic means and elemental analysis. From minimum inhibitory concentration (MIC) data, it has been observed that all the synthesized compounds exhibited good antibacterial activity in vitro.

N-alkylation of ethyl 1,4-dihydro-4-oxopyridine-3-carboxylates via their thallium(I) salts

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