Home Carboxys 7-Hydroxycoumarin-3-carboxylic acid

7-Hydroxycoumarin-3-carboxylic acid

CAS No.:
779-27-1
Catalog Number:
AG00ICWI
Molecular Formula:
C10H6O5
Molecular Weight:
206.1516
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
200mg
>98.0%(HPLC)
1 week
United States
$249
- +
1g
>98.0%(HPLC)
1 week
United States
$774
- +
Product Description
Catalog Number:
AG00ICWI
Chemical Name:
7-Hydroxycoumarin-3-carboxylic acid
CAS Number:
779-27-1
Molecular Formula:
C10H6O5
Molecular Weight:
206.1516
MDL Number:
MFCD00017491
IUPAC Name:
7-hydroxy-2-oxochromene-3-carboxylic acid
InChI:
InChI=1S/C10H6O5/c11-6-2-1-5-3-7(9(12)13)10(14)15-8(5)4-6/h1-4,11H,(H,12,13)
InChI Key:
LKLWLDOUZJEHDY-UHFFFAOYSA-N
SMILES:
Oc1ccc2c(c1)oc(=O)c(c2)C(=O)O
NSC Number:
115545
Properties
Complexity:
333  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
206.022g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
206.153g/mol
Monoisotopic Mass:
206.022g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
83.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.8  
Literature
Title Journal
Fluorescent assay for directed evolution of perhydrolases. Journal of biomolecular screening 20120701
Mechanism of radiation-induced reactions in aqueous solution of coumarin-3-carboxylic acid: effects of concentration, gas and additive on fluorescent product yield. Free radical research 20120701
TiO2 nanoparticles are phototoxic to marine phytoplankton. PloS one 20120101
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis. Bioorganic & medicinal chemistry letters 20101101
Photoactive yellow protein-based protein labeling system with turn-on fluorescence intensity. Journal of the American Chemical Society 20091125
Expanding the promiscuity of a natural-product glycosyltransferase by directed evolution. Nature chemical biology 20071001
Near infrared multiphoton-induced generation and detection of hydroxyl radicals in a biochemical system. Archives of biochemistry and biophysics 20070815
Evaluation of novel fluorogenic substrates for the detection of glycosidases in Escherichia coli and enterococci. Journal of applied microbiology 20061101
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
(Sub)-picosecond spectral evolution of fluorescence in photoactive proteins studied with a synchroscan streak camera system. Photochemistry and photobiology 20060101
Fungal modification of the hydroxyl radical detector coumarin-3-carboxylic acid. FEMS microbiology ecology 20031101
Detection of hydroxyl radicals produced by wood-decomposing fungi. FEMS microbiology ecology 20020401
Properties