Home Other Building Blocks 6-Amino-2H-chromen-2-one

6-Amino-2H-chromen-2-one

CAS No.:
14415-44-2
Catalog Number:
AG001J06
Molecular Formula:
C9H7NO2
Molecular Weight:
161.1574
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
250mg
95%
In Stock USA
United States
$48
- +
1g
98%
In Stock USA
United States
$75
- +
5g
98%
In Stock USA
United States
$225
- +
25g
98%
In Stock USA
United States
$900
- +
100g
98%
In Stock USA
United States
$2250
- +
Product Description
Catalog Number:
AG001J06
Chemical Name:
6-Amino-2H-chromen-2-one
CAS Number:
14415-44-2
Molecular Formula:
C9H7NO2
Molecular Weight:
161.1574
MDL Number:
MFCD00115435
IUPAC Name:
6-aminochromen-2-one
InChI:
InChI=1S/C9H7NO2/c10-7-2-3-8-6(5-7)1-4-9(11)12-8/h1-5H,10H2
InChI Key:
ZOJAINJCZSVZGW-UHFFFAOYSA-N
SMILES:
Nc1ccc2c(c1)ccc(=O)o2
UNII:
S9W3L9R2NA
Properties
Complexity:
225  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
161.048g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
161.16g/mol
Monoisotopic Mass:
161.048g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
52.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.7  
Literature
Title Journal
Radiationless deactivation of 6-aminocoumarin from the S1-ICT state in nonspecifically interacting solvents. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20120801
Design, synthesis and vasorelaxant evaluation of novel coumarin-pyrimidine hybrids. Bioorganic & medicinal chemistry 20111015
Changes in energy of three types of hydrogen bonds upon excitation of aminocoumarins determined from absorption solvatochromic experiments. Physical chemistry chemical physics : PCCP 20110621
Structure, photophysics, electrochemistry, DFT calculation, and in-vitro antioxidant activity of coumarin Schiff base complexes of Group 6 metal carbonyls. Journal of inorganic biochemistry 20110401
Synthesis of novel biologically active heterocyclic compounds from 2-oxo-2H-benzopyran-6-yl-imidazolidine. Acta poloniae pharmaceutica 20110101
Synthesis of biologically active 1'-(2-oxo-2H-benzopyran-6-yl)- 5'-hydroxy-2'-methylindole-3'-amido-2'-phenyl-thiazolidene-4'-ones. Acta poloniae pharmaceutica 20110101
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. Bioorganic & medicinal chemistry letters 20101101
Micronucleus induction and chromosomal aberration of 1- and 3-nitroazabenzo[a]pyrene and their N-oxides. Mutagenesis 20010501
Inhibition of HIV-1 IIIb replication in AA-2 and MT-2 cells in culture by two ligands of poly (ADP-ribose) polymerase: 6-amino-1,2-benzopyrone and 5-iodo-6-amino-1,2-benzopyrone. Biochemical and biophysical research communications 19911031
Properties