Home Other Building Blocks 1,5-Dihydroxyanthraquinone

1,5-Dihydroxyanthraquinone

CAS No.:
117-12-4
Catalog Number:
AG000DHU
Molecular Formula:
C14H8O4
Molecular Weight:
240.2109
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
85%
In Stock USA
United States
$33
- +
25g
85%
In Stock USA
United States
$54
- +
100g
85%
In Stock USA
United States
$122
- +
500g
85%
In Stock USA
United States
$260
- +
Product Description
Catalog Number:
AG000DHU
Chemical Name:
1,5-Dihydroxyanthraquinone
CAS Number:
117-12-4
Molecular Formula:
C14H8O4
Molecular Weight:
240.2109
MDL Number:
MFCD00001210
IUPAC Name:
1,5-dihydroxyanthracene-9,10-dione
InChI:
InChI=1S/C14H8O4/c15-9-5-1-3-7-11(9)14(18)8-4-2-6-10(16)12(8)13(7)17/h1-6,15-16H
InChI Key:
JPICKYUTICNNNJ-UHFFFAOYSA-N
SMILES:
Oc1cccc2c1C(=O)c1cccc(c1C2=O)O
EC Number:
204-175-6
UNII:
KPB60W5S3M
Properties
Complexity:
342  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
240.042g/mol
Formal Charge:
0
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
240.214g/mol
Monoisotopic Mass:
240.042g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
74.6A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.7  
Literature
Title Journal
Synchrotron radiation linear dichroism (SRLD) investigation of the electronic transitions of quinizarin, chrysazin, and anthrarufin. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20100915
Structure-activity relationships of anthraquinones on the suppression of DNA-binding activity of the aryl hydrocarbon receptor induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin. Journal of bioscience and bioengineering 20090301
Valence-state analysis through spectroelectrochemistry in a series of quinonoid-bridged diruthenium complexes [(acac)(2)Ru(mu-L)Ru(acac)(2)](n) (n=+2, +1, 0, -1, -2). Chemistry (Weinheim an der Bergstrasse, Germany) 20080101
C-Aryl glycosides via tandem intramolecular benzyne-furan cycloadditions. Total synthesis of vineomycinone B2 methyl ester. Journal of the American Chemical Society 20061025
Electrocoagulation of quinone pigments. Molecules (Basel, Switzerland) 20060714
Interaction of anthracene and its oxidative derivatives with human serum albumin. Acta biochimica Polonica 20060101
Six-coordinate titanium complexes of a tripodal aminetris(phenoxide) ligand: synthesis, structure, and dynamics. Inorganic chemistry 20050418
The specificity of cross-reactivity: promiscuous antibody binding involves specific hydrogen bonds rather than nonspecific hydrophobic stickiness. Protein science : a publication of the Protein Society 20031001
Synthesis of symmetrical 1,5-bisacyloxyanthraquinone derivatives and their dual activity of cytotoxicity and lipid peroxidation. Archiv der Pharmazie 20021201
Phytoestrogens from the roots of Polygonum cuspidatum (Polygonaceae): structure-requirement of hydroxyanthraquinones for estrogenic activity. Bioorganic & medicinal chemistry letters 20010723
Hydroxyquinones are competitive non-peptide inhibitors of HIV-1 proteinase. Biochimica et biophysica acta 19951115
Evaluation of the antiviral activity of anthraquinones, anthrones and anthraquinone derivatives against human cytomegalovirus. Antiviral research 19920101
Properties