Cas no 7044-91-9 (9,10-Anthracenedicarbaldehyde)
9,10-Anthracenedicarbaldehyde Chemical and Physical Properties
Names and Identifiers
-
- Anthracene-9,10-dicarbaldehyde
- ANTHRACENE-9,10-DICARBOXALDEHYDE
- AKOS AUF02026
- 9,10-Anthracenedicarbaldehyde
- Anthracene-9,10-biscarbaldehyde
- 9,10-Anthracenedicarboxaldehyde
- 9,10-anthracenedialdehyde
- 9,10-Diformylanthracene
- anthracene-8,10-dicarboxaldehyde
- SBRUFOSORMQHES-UHFFFAOYSA-N
- NSC529667
- PubChem15118
- 9,10-Anthracenedicarbaldehyde #
- 9,10-Anthracene dicarboxyaldehyde
- SBB071667
- 0910AC
- M
- DTXSID0064549
- SY033365
- Q27122534
- A836887
- AS-60222
- SCHEMBL986883
- YSWG147
- FT-0636340
- MFCD00045386
- 7044-91-9
- EINECS 230-322-9
- Q-200566
- anthracene-9,10-dialdehyde
- AKOS004114603
- CHEBI:51295
- NSC-529667
- CFX48CDY8V
- NSC 529667
- NS00037058
- T71250
- GEO-00236
- A2664
- DB-055415
- ALBB-014992
-
- MDL: MFCD00045386
- Inchi: 1S/C16H10O2/c17-9-15-11-5-1-2-6-12(11)16(10-18)14-8-4-3-7-13(14)15/h1-10H
- InChI Key: SBRUFOSORMQHES-UHFFFAOYSA-N
- SMILES: O=CC1C2C=CC=CC=2C(C=O)=C2C=CC=CC2=1
Computed Properties
- Exact Mass: 234.06800
- Monoisotopic Mass: 234.068079557g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 18
- Rotatable Bond Count: 2
- Complexity: 269
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 34.1
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: 3.3
Experimental Properties
- Color/Form: Not determined
- Density: 1.1480 (rough estimate)
- Melting Point: 242.0 to 246.0 deg-C
- Boiling Point: 471.2℃ at 760 mmHg
- Refractive Index: 1.6000 (estimate)
- PSA: 34.14000
- LogP: 3.61800
- Solubility: Not determined
- Sensitiveness: Sensitive to air
- λmax: 430(Diphenyl ether)(lit.)
9,10-Anthracenedicarbaldehyde Security Information
-
Symbol:
- Prompt:warning
- Hazard Statement: H315-H319
- Warning Statement: P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
- HazardClass:IRRITANT
9,10-Anthracenedicarbaldehyde Customs Data
- HS CODE:2912299000
- Customs Data:
China Customs Code:
2912299000Overview:
2912299000. Other cyclic aldehydes without other oxygen-containing groups. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:5.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to, Appearance of tetraformaldehyde
Summary:
2912299000. other cyclic aldehydes without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%
9,10-Anthracenedicarbaldehyde Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A229000380-1g |
Anthracene-9,10-dicarbaldehyde |
7044-91-9 | 95% | 1g |
$183.15 | 2023-09-01 | |
| Alichem | A229000380-5g |
Anthracene-9,10-dicarbaldehyde |
7044-91-9 | 95% | 5g |
$652.80 | 2023-09-01 | |
| BAI LING WEI Technology Co., Ltd. | 410917-1G |
Anthracene-9,10-dicarboxaldehyde, 98% |
7044-91-9 | 98% | 1G |
¥ 941 | 2022-04-26 | |
| BAI LING WEI Technology Co., Ltd. | 410917-5G |
Anthracene-9,10-dicarboxaldehyde, 98% |
7044-91-9 | 98% | 5G |
¥ 3563 | 2022-04-26 | |
| BAI LING WEI Technology Co., Ltd. | 148637-1G |
Anthracene-9,10-dicarboxaldehyde, 95% |
7044-91-9 | 95% | 1G |
¥ 828 | 2022-04-26 | |
| BAI LING WEI Technology Co., Ltd. | 148637-5G |
Anthracene-9,10-dicarboxaldehyde, 95% |
7044-91-9 | 95% | 5G |
¥ 2525 | 2022-04-26 | |
| TRC | A697695-250mg |
9,10-Anthracenedicarbaldehyde |
7044-91-9 | 250mg |
$ 121.00 | 2023-04-19 | ||
| TRC | A697695-500mg |
9,10-Anthracenedicarbaldehyde |
7044-91-9 | 500mg |
$ 207.00 | 2023-04-19 | ||
| TRC | A697695-1g |
9,10-Anthracenedicarbaldehyde |
7044-91-9 | 1g |
$ 315.00 | 2022-06-07 | ||
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | A866986-1g |
Anthracene-9,10-dicarboxaldehyde |
7044-91-9 | ≥98% | 1g |
989.00 | 2021-05-17 |
9,10-Anthracenedicarbaldehyde Suppliers
9,10-Anthracenedicarbaldehyde Related Literature
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Hong-Ju Yin,Yan-Ju Liu,Jie Gao,Ke-Zhi Wang Dalton Trans. 2017 46 3325
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Lin Qiu,Chengcheng Zhu,Huachao Chen,Ming Hu,Weijiang He,Zijian Guo Chem. Commun. 2014 50 4631
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Muhammad Faheem,Saba Aziz,Xiaofei Jing,Tingting Ma,Junyi Du,Fuxing Sun,Yuyang Tian,Guangshan Zhu J. Mater. Chem. A 2019 7 27148
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Alberth Lari,Mateusz B. Pitak,Simon J. Coles,Emma Bresco,Peter Belser,Andreas Beyeler,Melanie Pilkington,John D. Wallis CrystEngComm 2011 13 6978
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Nadine Popp,Thomas Homburg,Norbert Stock,Jürgen Senker J. Mater. Chem. A 2015 3 18492
Additional information on 9,10-Anthracenedicarbaldehyde
Recent Advances in the Research of 9,10-Anthracenedicarbaldehyde (CAS: 7044-91-9)
9,10-Anthracenedicarbaldehyde (CAS: 7044-91-9) is a significant organic compound widely used in the fields of chemical biology and pharmaceutical research. This compound, characterized by its anthracene backbone and dicarbaldehyde functional groups, has garnered attention for its versatile applications in organic synthesis, material science, and drug development. Recent studies have explored its potential as a building block for fluorescent probes, organic semiconductors, and bioactive molecules, making it a focal point in interdisciplinary research.
In the context of drug discovery, 9,10-Anthracenedicarbaldehyde has been investigated for its role in the synthesis of novel anticancer agents. A 2023 study published in the Journal of Medicinal Chemistry demonstrated its utility in constructing DNA-intercalating agents, which exhibit potent cytotoxicity against various cancer cell lines. The study highlighted the compound's ability to form stable complexes with DNA, leading to the disruption of cancer cell proliferation. These findings underscore its potential as a scaffold for developing next-generation chemotherapeutic agents.
Beyond its pharmaceutical applications, 9,10-Anthracenedicarbaldehyde has also been utilized in material science. Researchers have leveraged its photophysical properties to design organic light-emitting diodes (OLEDs) and sensors. A recent publication in Advanced Materials detailed the synthesis of a novel anthracene-based polymer using 9,10-Anthracenedicarbaldehyde as a key monomer. The resulting polymer exhibited exceptional electroluminescence efficiency, paving the way for advancements in optoelectronic devices.
In addition to its synthetic utility, the compound's mechanism of action has been a subject of rigorous investigation. A 2024 study in Chemical Communications employed density functional theory (DFT) calculations to elucidate the electronic structure and reactivity of 9,10-Anthracenedicarbaldehyde. The study revealed that the aldehyde groups play a critical role in modulating the compound's electrophilic character, which is essential for its reactivity in cross-coupling reactions. These insights provide a foundation for optimizing its use in catalytic processes.
Despite its promising applications, challenges remain in the large-scale synthesis and purification of 9,10-Anthracenedicarbaldehyde. Recent efforts have focused on developing greener synthetic routes to minimize environmental impact. For instance, a 2023 report in Green Chemistry described a solvent-free method for its preparation, achieving high yields with reduced waste generation. Such advancements align with the growing emphasis on sustainable chemistry in industrial and academic settings.
Looking ahead, the versatility of 9,10-Anthracenedicarbaldehyde continues to inspire innovation across multiple disciplines. Ongoing research aims to expand its applications in bioimaging, where its fluorescent properties could enable real-time tracking of cellular processes. Furthermore, collaborations between chemists and biologists are expected to uncover new therapeutic targets for this compound, solidifying its role in the future of chemical biology and medicine.
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