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Anthraquinone-2-carboxylic Acid - 10mM in DMSO, high purity , CAS No.117-78-2
Basic Description
Synonyms
Anthraquinone-2-carboxylic acid | 117-78-2 | 9,10-dioxo-9,10-dihydroanthracene-2-carboxylic acid | 2-Anthraquinonecarboxylic acid | 2-Carboxyanthraquinone | 9,10-Dioxoanthracene-2-carboxylic acid | 9,10-Anthraquinone 2-carboxylic acid | 9,10-Dihydro-9,10-dioxo-2-anthra
Specifications & Purity
10mM in DMSO
Storage Temp
Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description
application： Anthraquinone 2-carboxylic acid (AQ) as a novel electron shuttling mediator and attached electron relay for HRP. Efficient method for the generation of hydrogen peroxide by aerobic photooxidation of 2-propanol using anthraquinone-2-carboxylic acid and molecular oxygen is investigated.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Anthracenes
Subclass
Anthracenecarboxylic acids and derivatives
Intermediate Tree Nodes
Not available
Direct Parent
Anthracenecarboxylic acids
Alternative Parents
Anthraquinones Naphthalenecarboxylic acids Aryl ketones Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic homopolycyclic compounds
Substituents
Anthracene carboxylic acid - Anthraquinone - 9,10-anthraquinone - 2-naphthalenecarboxylic acid or derivatives - 2-naphthalenecarboxylic acid - Aryl ketone - Ketone - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound
Description
This compound belongs to the class of organic compounds known as anthracenecarboxylic acids. These are organic compounds containing a carboxylic acid group attached to an anthracene ring system.
External Descriptors
Not available
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Associated Targets(non-human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
IUPAC Name
9,10-dioxoanthracene-2-carboxylic acid
INCHI
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)
InChIKey
ASDLSKCKYGVMAI-UHFFFAOYSA-N
Smiles
C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C=C3)C(=O)O
Isomeric SMILES
C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C=C(C=C3)C(=O)O
WGK Germany
3
Molecular Weight
252.23
Beilstein
10(3)3640
Reaxy-Rn
2216475
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2216475&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Melt Point(°C)
287-289°C
Molecular Weight
252.220 g/mol
XLogP3
3.000
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
1
Exact Mass
252.042 Da
Monoisotopic Mass
252.042 Da
Topological Polar Surface Area
71.400 Ų
Heavy Atom Count
19
Formal Charge
0
Complexity
428.000
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
1.
Yuanyuan Song, Ziqi Wang, Yijing Long, Yang Mao, Feng Jiang, Yuanyuan Lu.
(2022)
2-Alkyl-anthraquinones inhibit Candida albicans biofilm via inhibiting the formation of matrix and hyphae. RESEARCH IN MICROBIOLOGY,
173
(103955).
2.
Man Chen, Quanhua Cai, Xiangyu Chen, Shaofu Huang, Qinyuan Feng, Tetsuro Majima, Raymond Jianxiong Zeng, Shungui Zhou.
(2022)
Anthraquinone-2-Sulfonate as a Microbial Photosensitizer and Capacitor Drives Solar-to-N2O Production with a Quantum Efficiency of Almost Unity. ENVIRONMENTAL SCIENCE & TECHNOLOGY,
56
(8):
(5161–5169).
3.
Yangyang Liu, Tao Wang, Xiaozhong Fang, Yue Deng, Hanyun Cheng, Aziz-Ur-Rahim Bacha, Iqra Nabi, Liwu Zhang.
(2020)
Brown carbon: An underlying driving force for rapid atmospheric sulfate formation and haze event. SCIENCE OF THE TOTAL ENVIRONMENT,
734
(139415).
4.
Lu-Yan Zhang, Chen-Hao Cui, Shan-Shan Yang, Yan Li, Han-Jun Sun, Nan-Qi Ren, Jie Ding.
(2025)
Advanced photocatalytic degradation of highly chlorinated organic wastewater using anthraquinone-modified carbon nitride: Driven by superoxide and dichloride radicals. CHEMICAL ENGINEERING JOURNAL,
(159409).
5.
Ning Xia, Fengli Gao, Gang Liu, Yong Chang, Lin Liu.
(2025)
Pyrroloquinoline quinone exhibiting peroxidase-mimicking property for colorimetric assays. ANALYTICA CHIMICA ACTA,
1335
(343468).
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5 Citations