252727
Anthraquinone-2-carboxylic acid
98%
Synonym(s):
9,10-Dihydro-9,10-dioxo-2-anthracenecarboxylic acid
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About This Item
Empirical Formula (Hill Notation):
C15H8O4
CAS Number:
Molecular Weight:
252.22
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
form
solid
mp
287-289 °C (lit.)
SMILES string
OC(=O)c1ccc2C(=O)c3ccccc3C(=O)c2c1
InChI
1S/C15H8O4/c16-13-9-3-1-2-4-10(9)14(17)12-7-8(15(18)19)5-6-11(12)13/h1-7H,(H,18,19)
InChI key
ASDLSKCKYGVMAI-UHFFFAOYSA-N
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Coupled Proton and Electron Transfer: Adsorbed Anthraquinone-2-carboxylic Acid Monolayers.
Forster RJ.
Journal of the Electrochemical Society, 144(4), 1165-1173 (1997)
Yiwen Zhu et al.
Materials (Basel, Switzerland), 13(16) (2020-08-17)
Antimicrobial and antiviral materials have attracted significant interest in recent years due to increasing occurrences of nosocomial infections and pathogenic microbial contamination. One method to address this is the combination of photoactive compounds that can produce reactive oxygen species (ROS)
K Kino et al.
Chemistry & biology, 8(4), 369-378 (2001-04-28)
The genome is constantly assaulted by oxidation reactions which are likely to be associated with oxygen metabolism, and oxidative lesions are generated by many types of oxidants. Such genotoxin-induced alterations in the genomic message have been implicated in aging and
Jie Sun et al.
Analytical chemistry, 90(11), 6660-6665 (2018-05-15)
To detect the redox state evolution during wound healing process, a redox-sensitive surface-enhanced Raman scattering (SERS) probe was constructed by attaching anthraquinone as a redox-sensitive molecule onto gold nanoshells, and the redox-sensitive SERS probes were loaded on one surface of
A Bielawska et al.
Polish journal of pharmacology, 53(3), 283-287 (2002-01-12)
A series of proline analogues of anthraquinone-2-carboxylic acid (1-3) were synthesized and evaluated for cytotoxic activity in the cultured breast cancer MCF-7 cells. The concentrations of 1, 2 and 3 needed to inhibit [3H]thymidine incorporation into DNA by 50% (IC50)
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