Home Other Building Blocks 2(1H)-Quinolinone, 3-hydroxy-4-phenyl-

2(1H)-Quinolinone, 3-hydroxy-4-phenyl-

CAS No.:
129-24-8
Catalog Number:
AG000YRM
Molecular Formula:
C15H11NO2
Molecular Weight:
237.2533
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1mg
≥99%
1 week
United States
$194
- +
50mg
98%
1 week
United States
$399
- +
Product Description
Catalog Number:
AG000YRM
Chemical Name:
2(1H)-Quinolinone, 3-hydroxy-4-phenyl-
CAS Number:
129-24-8
Molecular Formula:
C15H11NO2
Molecular Weight:
237.2533
MDL Number:
MFCD00965001
IUPAC Name:
3-hydroxy-4-phenyl-1H-quinolin-2-one
InChI:
InChI=1S/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)
InChI Key:
QSRVMXWVVMILDI-UHFFFAOYSA-N
SMILES:
Oc1c(=O)[nH]c2c(c1c1ccccc1)cccc2
UNII:
45493KS618
NSC Number:
656625
Properties
Complexity:
369  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
237.079g/mol
Formal Charge:
0
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
237.258g/mol
Monoisotopic Mass:
237.079g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
49.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.4  
Literature
Title Journal
Non-heme dioxygenase catalyzes atypical oxidations of 6,7-bicyclic systems to form the 6,6-quinolone core of viridicatin-type fungal alkaloids. Angewandte Chemie (International ed. in English) 20141117
Phylogeny of Penicillium and the segregation of Trichocomaceae into three families. Studies in mycology 20111115
Phylogeny and nomenclature of the genus Talaromyces and taxa accommodated in Penicillium subgenus Biverticillium. Studies in mycology 20111115
3-Hy-droxy-4-(3-hy-droxy-phen-yl)-2-quinolone monohydrate. Acta crystallographica. Section E, Structure reports online 20110801
[Efficient construction of nitrogen-containing heterocycles utilizing CN functional groups and its application to the synthesis of natural products]. Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan 20110101
A concise and versatile synthesis of viridicatin alkaloids from cyanoacetanilides. Organic letters 20090402
[The biosynthesis of low-molecular-weight nitrogen-containing secondary metabolite-alkaloids by the resident strains of Penicillium chrysogenum and Penicillium expansum isolated on the board of the Mir space station ]. Mikrobiologiia 20020101
Isolation and characterization of the fungal metabolite 3-O-methylviridicatin as an inhibitor of tumour necrosis factor alpha-induced human immunodeficiency virus replication. Antiviral chemistry & chemotherapy 19980301
Properties