Home Other Building Blocks 1,4-Anthraquinone

1,4-Anthraquinone

CAS No.:
635-12-1
Catalog Number:
AG0032M6
Molecular Formula:
C14H8O2
Molecular Weight:
208.2121
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$83
- +
5g
95%
In Stock USA
United States
$261
- +
25g
95%
In Stock USA
United States
$986
- +
Product Description
Catalog Number:
AG0032M6
Chemical Name:
1,4-Anthraquinone
CAS Number:
635-12-1
Molecular Formula:
C14H8O2
Molecular Weight:
208.2121
MDL Number:
MFCD00013724
IUPAC Name:
anthracene-1,4-dione
InChI:
InChI=1S/C14H8O2/c15-13-5-6-14(16)12-8-10-4-2-1-3-9(10)7-11(12)13/h1-8H
InChI Key:
LSOTZYUVGZKSHR-UHFFFAOYSA-N
SMILES:
O=C1C=CC(=O)c2c1cc1ccccc1c2
EC Number:
211-228-7
NSC Number:
104530
Properties
Complexity:
322  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
208.052g/mol
Formal Charge:
0
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
208.216g/mol
Monoisotopic Mass:
208.052g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
34.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3  
Literature
Title Journal
Comparative developmental toxicity of environmentally relevant oxygenated PAHs. Toxicology and applied pharmacology 20130901
Self-assembled hexanuclear organometallic cages: synthesis, characterization, and host-guest properties. Chemistry, an Asian journal 20120601
Tautomerism in 11-hydroxyaklavinone: a DFT study. TheScientificWorldJournal 20120101
Lateral extension of π conjugation along the bay regions of bisanthene through a Diels-Alder cycloaddition reaction. Chemistry (Weinheim an der Bergstrasse, Germany) 20111216
Tunneling currents that increase with molecular elongation. Journal of the American Chemical Society 20111005
Concise total syntheses of variecolortides A and B through an unusual hetero-Diels-Alder reaction. Angewandte Chemie (International ed. in English) 20110207
Free radical reaction between 2-benzoyl-1,4-benzoquinones and 1,3-dicarbonyl compounds. Organic & biomolecular chemistry 20091007
6,7-Dimeth-oxy-1,4-anthraquinone. Acta crystallographica. Section E, Structure reports online 20080901
Synthesis of zirconia-immobilized copper chelates for catalytic decomposition of hydrogen peroxide and the oxidation of polycyclic aromatic hydrocarbons. Chemosphere 20080801
Novel substituted 1,4-anthracenediones with antitumor activity directly induce permeability transition in isolated mitochondria. International journal of oncology 20071101
Syntheses, molecular targets and antitumor activities of novel triptycene bisquinones and 1,4-anthracenedione analogs. Anti-cancer agents in medicinal chemistry 20060701
1,4,9,10-Anthradiquinone as precursor for antitumor compounds. Bioorganic & medicinal chemistry 20060515
Alpha-glucosidase inhibitory anthranols, kenganthranols A-C, from the stem bark of Harungana madagascariensis. Journal of natural products 20060201
Rapid collapse of mitochondrial transmembrane potential in HL-60 cells and isolated mitochondria treated with anti-tumor 1,4-anthracenediones. Anti-cancer drugs 20051001
Proton translocation in monomolecular Langmuir-Blodgett films including 2-naphthol and 1,4-anthraquinone derivatives. The journal of physical chemistry. B 20050407
Role of LHCII organization in the interaction of substituted 1,4-anthraquinones with thylakoid membranes. Journal of photochemistry and photobiology. B, Biology 20050201
Synthetic 1,4-anthracenedione analogs induce cytochrome c release, caspase-9, -3, and -8 activities, poly(ADP-ribose) polymerase-1 cleavage and internucleosomal DNA fragmentation in HL-60 cells by a mechanism which involves caspase-2 activation but not Fas signaling. Biochemical pharmacology 20040201
A new approach to evaluating the extent of Michael adduct formation to PAH quinones: tetramethylammonium hydroxide (TMAH) thermochemolysis with GC/MS. Chemical research in toxicology 20031101
Identification of toxic products of anthracene photomodification in simulated sunlight. Environmental toxicology and chemistry 20031001
Influence of substituted 1,4-anthraquinones on the chlorophyll fluorescence and photochemical activity of pea thylakoid membranes. Journal of photochemistry and photobiology. B, Biology 20030101
Electronic structure of the lowest excited triplet state of 5,12-naphthacenequinone. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20020401
Excited-state dynamical behavior of 1,4-anthraquinone in a fluid solution. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20020115
Synthetic 1,4-anthracenediones, which block nucleoside transport and induce DNA fragmentation, retain their cytotoxic efficacy in daunorubicin-resistant HL-60 cell lines. Anti-cancer drugs 20011101
Properties