9-Anthroic acid - Moligand™, ≥98% , Channel blocker of CaCC;Channel blocker of ClC-1, CAS No.723-62-6, Channel blocker of CaCC;Channel blocker of ClC-1

CAS: 723-62-6 Cat. No.: A101360 Molecular Weight: 222.24 Beilstein Registry Number: 1875336 EC Number: 211-964-9
AVAILABLE TO ORDER
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
CAS-723-62-6 | XGWFJBFNAQHLEF-UHFFFAOYSA- | anthracene-9-carboxylic acid | HMS3675L16 | Tox21_202942 | 7VK69492FV | (9-AC) | FT-0621619 | NCGC00024906-03 | KBioGR_001569 | Spectrum4_000875 | 9-Anthracenecarboxylic acid | A0690 | KBio3_002733 | DTXCID60293
Storage
Room temperature,Cool
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
A101360-1g
5
$9.90
5g
A101360-5g
5
$11.90
25g
A101360-25g
4
$23.90
100g
A101360-100g
2
$71.90
500g
A101360-500g
1
$325.90
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Cool Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 14 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

application:

9-Anthracenecarboxylic acid can be used as a starting material to synthesize:

9-Cyanoanthracene by reacting with cyanohydrins in the presence of a palladium catalyst.

6-Chloro-8-(9-anthracenyl)-9H-purine by Ag/SiO2 catalyzed reaction one-pot reaction with 6-chloro-4,5-pyrimidinediamine.

It can also be used as a cross-linking agent to functionalize organic second-order nonlinear optical materials to enhance poling efficiency and temporal stability.

Specifications

Synonyms
CAS-723-62-6 | XGWFJBFNAQHLEF-UHFFFAOYSA- | anthracene-9-carboxylic acid | HMS3675L16 | Tox21_202942 | 7VK69492FV | (9-AC) | FT-0621619 | NCGC00024906-03 | KBioGR_001569 | Spectrum4_000875 | 9-Anthracenecarboxylic acid | A0690 | KBio3_002733 | DTXCID60293
Specifications & Purity
Moligand™, ≥98%
Biochemical and Physiological Mechanisms
Cl-transport inhibitor with a moderate to strong inhibitory action on PKA activated cardiac IcI.
Storage
Room temperature, Cool
Shipped In
Normal
Grade
Moligand™
Action Type
CHANNEL BLOCKER
Mechanism of action
Channel blocker of CaCC;Channel blocker of ClC-1
Purity
≥98%
Names and Identifiers
Pubchem Sid488179675
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488179675
Canonical SmilesC1=CC=C2C(=C1)C=C3C=CC=CC3=C2C(=O)O
IUPAC Nameanthracene-9-carboxylic acid
InChIKeyXGWFJBFNAQHLEF-UHFFFAOYSA-N
INCHI1S/C15H10O2/c16-15(17)14-12-7-3-1-5-10(12)9-11-6-2-4-8-13(11)14/h1-9H,(H,16,17)
Isomeric SMILES C1=CC=C2C(=C1)C=C3C=CC=CC3=C2C(=O)O
WGK Germany 3
RTECS CB8764000
Molecular Weight 222.24
Beilstein 1875336
Reaxy-Rn 1875336
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1875336&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassAnthracenes
SubclassAnthracenecarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentAnthracenecarboxylic acids
Alternative Parents Naphthalenecarboxylic acids  Monocarboxylic acids and derivatives  Carboxylic acids  Organooxygen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Anthracene carboxylic acid - 1-naphthalenecarboxylic acid or derivatives - 1-naphthalenecarboxylic acid - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound
DescriptionThis 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 anthroic acid
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
CLCN1 Tbio Chloride channel protein 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ANO1 Tclin Anoctamin-1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
GLA Tclin Alpha-galactosidase A (5444 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC16A1 Tchem Monocarboxylate transporter 1 (146 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
USP1 Tchem Ubiquitin carboxyl-terminal hydrolase 1 (22556 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC16A7 Tchem Monocarboxylate transporter 2 (11 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Caenorhabditis elegans (1055 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Meloidogyne incognita (862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Heterorhabditis bacteriophora (7 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

24 results found

Lot NumberCertificate TypeDateItem
G1813059Certificate of AnalysisFeb 05, 2026 A101360
C2226544Certificate of AnalysisJan 19, 2026 A101360
C2226546Certificate of AnalysisJan 19, 2026 A101360
L2517559Certificate of AnalysisNov 22, 2025 A101360
L2517558Certificate of AnalysisNov 22, 2025 A101360
L2508180Certificate of AnalysisNov 22, 2025 A101360
L2508179Certificate of AnalysisNov 22, 2025 A101360
G2517681Certificate of AnalysisAug 23, 2024 A101360
I2406075Certificate of AnalysisAug 23, 2024 A101360
I2406074Certificate of AnalysisAug 23, 2024 A101360
I2406073Certificate of AnalysisAug 23, 2024 A101360
H2419326Certificate of AnalysisAug 05, 2024 A101360
I2529013Certificate of AnalysisJul 10, 2024 A101360
I2529463Certificate of AnalysisJul 10, 2024 A101360
D2303463Certificate of AnalysisFeb 17, 2023 A101360
D2303460Certificate of AnalysisFeb 17, 2023 A101360
D2303458Certificate of AnalysisFeb 17, 2023 A101360
D2303457Certificate of AnalysisFeb 17, 2023 A101360
D2303456Certificate of AnalysisFeb 17, 2023 A101360
D2303455Certificate of AnalysisFeb 17, 2023 A101360
D2303444Certificate of AnalysisFeb 17, 2023 A101360
B2321246Certificate of AnalysisMar 07, 2022 A101360
C2226545Certificate of AnalysisMar 07, 2022 A101360
C2226547Certificate of AnalysisMar 07, 2022 A101360

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Chemical and Physical Properties
SolubilitySolvent:ethanol, Max Conc. mg/mL: None, Max Conc. mM: 10; Solvent:DMSO, Max Conc. mg/mL: None, Max Conc. mM: 100
Melt Point(°C)213-217 °C
Molecular Weight222.240 g/mol
XLogP33.800
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass222.068 Da
Monoisotopic Mass222.068 Da
Topological Polar Surface Area37.300 Ų
Heavy Atom Count17
Formal Charge0
Complexity277.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Shida Luo, Yuting Zhang, Yanshen Zhu, Xiao-Juan Wang, Xia Ran, Yulu He, Yanmin Kuang, Zhen Chi, Lijun Guo.  (2023)  Size-Regulated Hole and Triplet Energy Transfer from CdSe Quantum Dots to Organic Acceptors for Enhancing Singlet Oxygen Generation.  INORGANIC CHEMISTRY,      [PMID:37934916] [10.1021/acs.inorgchem.3c03134]
2. Ren-Man Zhu, Zi-Xuan Chang, Wen-Jian Zhang, Chun-Yan Hong.  (2023)  Polymerization-Induced Self-Assembly with Assistance of Aromatic Interactions Facilitates the Formation of Polymeric Nanotubes.  MACROMOLECULES,      [PMID:] [10.1021/acs.macromol.3c00302]
3. Zhen Chi, Jia Xu, Shida Luo, Xia Ran, Xiaojuan Wang, Pingan Liu, Yulu He, Yanmin Kuang, Lijun Guo.  (2023)  Triplet generation at the CdTe quantum dot/anthracene interface mediated by hot and thermalized electron exchange for enhanced production of singlet oxygen.  PHYSICAL CHEMISTRY CHEMICAL PHYSICS,  25  (12): (8913-8920).  [PMID:36916640] [10.1039/D3CP00021D]
4. Yongqi Liu, Lei Wang, Jingtao Jiang, Xiangke Wang, Chenghao Dai, Gengsheng Weng.  (2022)  Fast Healing of Covalently Cross-Linked Polymeric Hydrogels by Interfacially Ignited Fast Gelation.  MACROMOLECULES,      [PMID:] [10.1021/acs.macromol.2c02065]
5. Kui Li, Miao Sun, Wei-De Zhang.  (2018)  Polycyclic aromatic compounds-modified graphitic carbon nitride for efficient visible-light-driven hydrogen evolution.  CARBON,      [PMID:] [10.1016/j.carbon.2018.03.089]
6. Jie Gao, Caihong Wang, Hongliang Tan.  (2017)  Dual-emissive polystyrene@zeolitic imidazolate framework-8 composite for ratiometric detection of singlet oxygen.  Journal of Materials Chemistry B,  (46): (9175-9182).  [PMID:32264599] [10.1039/C7TB02684F]
7. Yinhui Yi, Odoom Jibrael Kingsford, Mwenze Nkulu Fiston, Junjuan Qian, Zhenjiang Liu, Lirong Liu, Gangbing Zhu.  (2017)  Perylenetetracarboxylic acid noncovalently functionalizes carbon nanohorn nanohybrids for electrochemical sensing of 4,4′-diaminobiphenyl.  JOURNAL OF ELECTROANALYTICAL CHEMISTRY,      [PMID:] [10.1016/j.jelechem.2017.07.025]
8. Liu Hongmei, Chang Hong, Lv Jia, Jiang Cong, Li Zhenxi, Wang Fei, Wang Hui, Wang Mingming, Liu Chongyi, Wang Xinyu, Shao Naimin, He Bingwei, Shen Wanwan, Zhang Qiang, Cheng Yiyun.  (2016)  Screening of efficient siRNA carriers in a library of surface-engineered dendrimers.  Scientific Reports,  (1): (1-11).  [PMID:27121799] [10.1038/srep25069]
9. Chao Xu, Yong Chen, Heng-Yi Zhang, Yu Liu.  (2015)  Photo-induced secondary assembly of bis(terpyridyl)dibenzo-24-crown-8/Zn2+ supramolecular polymer.  JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY,      [PMID:] [10.1016/j.jphotochem.2015.04.014]
10. Zhenxing Chen, Lifeng Gui, Hao Wang, Xiaohui Lu, Congcong Wu, Xiaojie Yang, Yanyan Li, Li Zhao, Shimin Wang.  (2025)  Bifunctional π conjugated g-C3N4 for enhancing the efficiency and stability of carbon-based perovskite solar cells.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2025.131797]
11. Kai Gou, Lei Wang, Minghui Wei, Jingtao Jiang, Gengsheng Weng.  (2024)  Biomorphogenesis-Inspired Three-Dimensional Shape Transformation of Bilayer Polymer Sheets.  CHEMISTRY OF MATERIALS,      [PMID:] [10.1021/acs.chemmater.4c00049]
12. Yajun Xu, Jialong Zhang, Xiangfei Zheng, Liang Xu, Jingcheng Liu.  (2024)  Synthesis of copolymer containing anthracene group and its application in bottom anti-reflective coatings for KrF photoresist.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2024.109002]
13. Jie Zhong, Hang Wei, Jian-Xiong Xie, Yu-Hui Wu, Bing Tang, Qi Zou, Peng-Ran Guo, Zhi-Liang Chen.  (2024)  Uptake, subcellular distribution, and fate of tetracycline in two wetland plants supplemented with microbial agents: Effect and mechanism.  JOURNAL OF ENVIRONMENTAL MANAGEMENT,      [PMID:38879966] [10.1016/j.jenvman.2024.121428]
14. Pengpeng Li, Jiahao Zhang, Yike Jin, Zifan Xu, Guohua Sun.  (2026)  Spontaneous Symmetry Breaking to Amplified Chirality: Biomimetic Helical Nanofibers for High-Performance Circularly Polarized Luminescence.  ADVANCED FUNCTIONAL MATERIALS,      [PMID:] [10.1002/adfm.74486]
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