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Home Other Building Blocks 7-Hydroxy-4-phenyl-2H-chromen-2-one

7-Hydroxy-4-phenyl-2H-chromen-2-one

CAS No.:
2555-30-8
Catalog Number:
AG00BFL2
Molecular Formula:
C15H10O3
Molecular Weight:
238.2381
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
1 week
United States
$98
- +
5g
1 week
United States
$289
- +
10g
1 week
United States
$439
- +
25g
1 week
United States
$841
- +
Product Description
Catalog Number:
AG00BFL2
Chemical Name:
7-Hydroxy-4-phenyl-2H-chromen-2-one
CAS Number:
2555-30-8
Molecular Formula:
C15H10O3
Molecular Weight:
238.2381
MDL Number:
MFCD00024080
IUPAC Name:
7-hydroxy-4-phenylchromen-2-one
InChI:
InChI=1S/C15H10O3/c16-11-6-7-12-13(10-4-2-1-3-5-10)9-15(17)18-14(12)8-11/h1-9,16H
InChI Key:
IVJMJRRORVMRJJ-UHFFFAOYSA-N
SMILES:
Oc1ccc2c(c1)oc(=O)cc2c1ccccc1
UNII:
L0487H6Q0H
NSC Number:
78474
Properties
Complexity:
355  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
238.063g/mol
Formal Charge:
0
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
238.242g/mol
Monoisotopic Mass:
238.063g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
46.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.2  
Literature
Title Journal
Biotransformation of hydroxycoumarin derivatives by cultured suspension cells of Catharanthus roseus. Die Pharmazie 20120501
Synthesis and anti-inflammatory effects of a series of novel 7-hydroxycoumarin derivatives. European journal of medicinal chemistry 20110901
Physicochemical characterization and antioxidant activity of melanin from a novel strain of Aspergillus bridgeri ICTF-201. Letters in applied microbiology 20110901
6,7-Dihydroxy-4-phenylcoumarin as inhibitor of aldose reductase 2. Bioorganic & medicinal chemistry letters 20101001
Microsphere-based protease assays and screening application for lethal factor and factor Xa. Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501
Synthesis of potential antidipsotropic isoflavones: inhibitors of the mitochondrial monoamine oxidase-aldehyde dehydrogenase pathway. Journal of medicinal chemistry 20010927
Properties