Home Aldehydes 7-Hydroxy-4-methyl-2-oxo-2H-chromene-8-carbaldehyde

7-Hydroxy-4-methyl-2-oxo-2H-chromene-8-carbaldehyde

CAS No.:
14003-96-4
Catalog Number:
AG001BYN
Molecular Formula:
C11H8O4
Molecular Weight:
204.1788
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
10mg
95%
In Stock USA
United States
$75
- +
50mg
95%
In Stock USA
United States
$188
- +
Product Description
Catalog Number:
AG001BYN
Chemical Name:
7-Hydroxy-4-methyl-2-oxo-2H-chromene-8-carbaldehyde
CAS Number:
14003-96-4
Molecular Formula:
C11H8O4
Molecular Weight:
204.1788
MDL Number:
MFCD12027255
IUPAC Name:
7-hydroxy-4-methyl-2-oxochromene-8-carbaldehyde
InChI:
InChI=1S/C11H8O4/c1-6-4-10(14)15-11-7(6)2-3-9(13)8(11)5-12/h2-5,13H,1H3
InChI Key:
RTHHSXOVIJWFQP-UHFFFAOYSA-N
SMILES:
O=Cc1c(O)ccc2c1oc(=O)cc2C
Properties
Complexity:
321  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
204.042g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
204.181g/mol
Monoisotopic Mass:
204.042g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
63.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.5  
Literature
Title Journal
Synthesis of novel tricyclic chromenone-based inhibitors of IRE-1 RNase activity. Journal of medicinal chemistry 20140522
Synthesis, spectroscopic characterization and biological evaluation studies of Schiff's base derived from naphthofuran-2-carbohydrazide with 8-formyl-7-hydroxy-4-methyl coumarin and its metal complexes. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20121201
8-Formyl-4-methyl-2-oxo-2H-chromen-7-yl 4-methyl-benzenesulfonate. Acta crystallographica. Section E, Structure reports online 20110601
Synthesis, physico-chemical investigations of Co(II), Ni(II) and Cu(II) complexes and their in vitro microbial, cytotoxic, DNA cleavage studies. Journal of enzyme inhibition and medicinal chemistry 20100601
DNA cleavage and in vitro antimicrobial studies of Co(II), Ni(II), and Cu(II) complexes with ONNO donor Schiff bases: synthesis, spectral characterization, and electrochemical studies. Journal of enzyme inhibition and medicinal chemistry 20100201
Synthesis, characterization, DNA cleavage and in vitro antimicrobial studies of La(III), Th(IV) and VO(IV) complexes with Schiff bases of coumarin derivatives. European journal of medicinal chemistry 20090701
Synthesis, spectral characterization, in vitro microbial and cytotoxic studies of lanthanum(III) and thorium(IV) complexes with 1,2,4-triazole Schiff bases. Journal of enzyme inhibition and medicinal chemistry 20090601
Synthesis, spectral characterization and in vitro biological studies of Co(II), Ni(II) and Cu(II) complexes with 1,2,4-triazole Schiff bases. Journal of enzyme inhibition and medicinal chemistry 20090401
Synthesis, spectral characterization, in vitro antibacterial, antifungal and cytotoxic activities of Co(II), Ni(II) and Cu(II) complexes with 1,2,4-triazole Schiff bases. European journal of medicinal chemistry 20081201
Coumarin as attractive casein kinase 2 (CK2) inhibitor scaffold: an integrate approach to elucidate the putative binding motif and explain structure-activity relationships. Journal of medicinal chemistry 20080227
Properties