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CAS No 129-24-8 , 2(1H)-Quinolinone,3-hydroxy-4-phenyl-

  • Name: 2(1H)-Quinolinone,3-hydroxy-4-phenyl-
  • Synonyms: 3-Hydroxy-4-phenylcarbostyril; Viridicatine;Carbostyril,3-hydroxy-4-phenyl- (7CI,8CI); Viridicatin;2(1H)-Quinolinone,3-hydroxy-4-phenyl-;3-Hydroxy-4-phenylquinolin-2-one; 2,3-Dihydroxy-4-phenylquinoline; NSC 656625;3-Hydroxy-4-phenyl-2-quinolone; 3-Hydroxy-4-phenyl-2(1H)-quinolinone;2,6-Dihydroxy-4-phenylquinoline;
  • CAS Registry Number:
  • Flash Point: 242.1°C
  • Boiling Point: 476.7°Cat760mmHg
  • Density: 1.323g/cm3
  • Refractive index: 1.677
  • Flash Point: 242.1°C
  • Molecular Weight: 0
  • InChI: InChI=1/C15H11NO2/c17-14-13(10-6-2-1-3-7-10)11-8-4-5-9-12(11)16-15(14)18/h1-9,17H,(H,16,18)
  • Molecular Formula: C15H11 N O2
  • Molecular Structure:CAS No:129-24-8 2(1H)-Quinolinone,3-hydroxy-4-phenyl-
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129-24-8 VIRIDICATIN

  • China Nanjing Chemlin Chemical Industry Co.,Ltd. [Manufacturer]
  • Tel: +86 25 8369-7070/ +86 138 51816776 (Mobile)
  • Fax: +86 25 8345-3275
  • Address: Rm.902 Longyin Plaza,
    No. 217 Zhongshan Rd.
    (N)Nanjing 210009,China null,nullChina
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129-24-8 VIRIDICATIN

  • Germany Cfm Oskar Tropitzsch [Manufacturer]
  • Tel: +49-9231-9619-0
  • Fax: +49-9231-9619-60
  • Address: Cfm Oskar Tropitzsch
    Waldershofer Str. 49-51
    95615 Marktredwitz
    Germany null,nullGermany
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References of 2(1H)-Quinolinone,3-hydroxy-4-phenyl-
Title: Viridicatin
CAS Registry Number: 129-24-8
CAS Name: 3-Hydroxy-4-phenyl-2(1H)-quinolinone
Synonyms: 3-hydroxy-4-phenylcarbostyril; 2,3-dihydroxy-4-phenylquinoline
Molecular Formula: C15H11NO2
Molecular Weight: 237.25
Percent Composition: C 75.94%, H 4.67%, N 5.90%, O 13.49%
Literature References: Antibiotic substance from the mycelium of Penicillium viridicatum Westling, the chief mold on stored corn: Cunningham, Freeman, Biochem. J. 53, 328 (1953); from various strains of P. cyclopium Westling: Bracken et al., ibid. 57, 587 (1954); from P. puberulum Bainier: Austin, Meyers, J. Chem. Soc. 1964, 1197. Biosynthesis: Luckner, Tetrahedron Lett. 1962, 1035; Luckner, Mothes, Arch. Pharm. 296, 18 (1963); Framm et al., Eur. J. Biochem. 37, 78 (1973). Synthesis: Eistert, Selzer, Z. Naturforsch. 17b, 202 (1962). Mass spectra: Luckner et al., Tetrahedron 25, 2575 (1969). Antibacterial activity and inhibitory effect on plant growth: Taniguchi, Satomura, Agric. Biol. Chem. 34, 506 (1970).
Properties: Lustrous needles from methanol or ethanol, mp 268°. Sublimes unchanged in high vacuum at 160-170°. Very weak acid. uv and ir curves: Cunningham, Freeman, loc. cit. Practically insol in water, aq NaHCO3. Sparingly sol in cold organic solvents, cold concd HCl, dil mineral acids; sol in cold, aq 2N KOH, glacial acetic acid.
Melting point: mp 268°
 
Derivative Type: Sodium salt
Molecular Formula: C15H10NNaO2
Molecular Weight: 259.24
Percent Composition: C 69.50%, H 3.89%, N 5.40%, Na 8.87%, O 12.34%
Properties: Prismatic needles from aq NaOH, dec 260-265°. Sol in water.
 
Derivative Type: Monoacetylviridicatin
Molecular Formula: C17H13NO3
Molecular Weight: 279.29
Percent Composition: C 73.11%, H 4.69%, N 5.02%, O 17.19%
Properties: Crystals from aq ethanol, mp 200-201°. Dec slowly on standing.
Melting point: mp 200-201°
 
Derivative Type: O,O-Dimethylviridicatin
Molecular Formula: C17H15NO2
Molecular Weight: 265.31
Percent Composition: C 76.96%, H 5.70%, N 5.28%, O 12.06%
Properties: Plates from ethanol, mp 86-87°.
Melting point: mp 86-87°
 
Derivative Type: O,N-Dimethylviridicatin
Molecular Formula: C17H15NO2
Molecular Weight: 265.31
Percent Composition: C 76.96%, H 5.70%, N 5.28%, O 12.06%
Properties: Plates from ethanol, mp 197-198°.
Melting point: mp 197-198°