Atomfair Quinfamide Amenide, Amenox, Win 40014 C16H13Cl2NO4 CAS 62265-68-3

Quinfamide (CAS No. 62265-68-3) is a synthetic organic compound with the molecular formula C16H13Cl2NO4and the IUPAC name [1-(2,2-dichloroacetyl)-3,4-dihydro-2H-quinolin-6-yl] furan-2-carboxylate . This high-purity chemical is supplied as a fine white to off-white crystalline powder, rigorously tested for identity, purity, and stability to meet the stringent requirements of pharmaceutical and biochemical research. Quinfamide is a potent antiprotozoal agent with documented efficacy against intestinal parasites, making it a valuable reference standard in parasitology studies. Our product is packaged under inert conditions to ensure long-term stability and is available in quantities ranging from milligrams to kilograms to support both small-scale research and industrial applications.…

Description

Quinfamide (CAS No. 62265-68-3) is a synthetic organic compound with the molecular formula C16H13Cl2NO4 and the IUPAC name [1-(2,2-dichloroacetyl)-3,4-dihydro-2H-quinolin-6-yl] furan-2-carboxylate. This high-purity chemical is supplied as a fine white to off-white crystalline powder, rigorously tested for identity, purity, and stability to meet the stringent requirements of pharmaceutical and biochemical research. Quinfamide is a potent antiprotozoal agent with documented efficacy against intestinal parasites, making it a valuable reference standard in parasitology studies. Our product is packaged under inert conditions to ensure long-term stability and is available in quantities ranging from milligrams to kilograms to support both small-scale research and industrial applications. Each batch is accompanied by comprehensive analytical documentation including HPLC chromatograms, MSDS, and Certificate of Analysis.

Properties

  • CAS Number: 62265-68-3
  • Complexity: 459
  • IUPAC Name: [1-(2,2-dichloroacetyl)-3,4-dihydro-2H-quinolin-6-yl] furan-2-carboxylate
  • InChI: InChI=1S/C16H13Cl2NO4/c17-14(18)15(20)19-7-1-3-10-9-11(5-6-12(10)19)23-16(21)13-4-2-8-22-13/h2,4-6,8-9,14H,1,3,7H2
  • InChI Key: SBJGFIXQRZOVTO-UHFFFAOYSA-N
  • Exact Mass: 353.0221633
  • Molecular Formula: C16H13Cl2NO4
  • Molecular Weight: 354.2
  • SMILES: C1CC2=C(C=CC(=C2)OC(=O)C3=CC=CO3)N(C1)C(=O)C(Cl)Cl
  • Topological: 59.8
  • Monoisotopic Mass: 353.0221633
  • Synonyms: Quinfamide, 62265-68-3, Amenide, Amenox, Win 40014, Quinfamido, Quinfamida, 2-Furancarboxylic acid, 1-(2,2-dichloroacetyl)-1,2,3,4-tetrahydro-6-quinolinyl ester, 1-(Dichloroacetyl)-6-(2-furoyloxy)-1,2,3,4-tetrahydroquinoline, WIN-40014, [1-(2,2-dichloroacetyl)-3,4-dihydro-2H-quinolin-6-yl] furan-2-carboxylate, 2-Furancarboxylic acid, 1-(dichloroacetyl)-1,2,3,4-tetrahydro-6-quinolinyl ester, O1ZB1046R1, 2-Furoic acid ester with 1-(dichloroacetyl)-1,2,3,4-tetrahydro-6-quinolinol, Quinfamidum, Quinfamide [USAN:INN], Quinfamidum [INN-Latin], 1-(2,2-dichloroacetyl)-1,2,3,4-tetrahydroquinolin-6-yl furan-2-carboxylate, Quinfamido [INN-Spanish], EINECS 263-478-1, BRN 1554485, UNII-O1ZB1046R1, Amenide (TN), MFCD00864662, QUINFAMIDE [MI], QUINFAMIDE [INN], Quinfamide (USAN/INN), QUINFAMIDE [USAN], QUINFAMIDE [MART.], QUINFAMIDE [WHO-DD], SCHEMBL635943, CHEMBL2107014, DTXSID90211320, CHEBI:135493, SBJGFIXQRZOVTO-UHFFFAOYSA-N, BCP10697, EX-A3370, AKOS030227997, DB12780, FQ27375, AS-73999, DA-67075, HY-119826, CS-0078079, NS00034988, A10941, D00641, Q21098930, 2-Furancarboxylic acid 1-(2,2-dichloroacetyl)-1,2,3,4-tetrahydro-6-quinolinyl ester;1-(Dichloroacetyl)-6-(2-furoyloxy)-1,2,3,4-tetra hydro-6-quinoline;Amenide

Application

Quinfamide is primarily utilized as an antiprotozoal agent in pharmacological research, particularly for studying its effects on intestinal parasites like Entamoeba histolytica. The compound demonstrates potent amebicidal activity through inhibition of protein synthesis in target organisms. Researchers employ quinfamide as a reference compound in drug development programs for parasitic infections. Its mechanism of action and structure-activity relationships make it valuable for medicinal chemistry optimization studies.

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