Cas no 54299-17-1 (1,4-Bis(4-phenoxybenzoyl)benzene)
1,4-Bis(4-phenoxybenzoyl)benzene Chemical and Physical Properties
Names and Identifiers
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- 1,4-Phenylenebis((4-phenoxyphenyl)methanone)
- [4-(4-phenoxybenzoyl)phenyl]-(4-phenoxyphenyl)methanone
- 1,4-BIS(4-PHENOXYBENZOYL)BENZENE
- 1,4-bis(4'-phenoxybenzoyl)benzene
- 4,4'-Diphenoxyterephthalophenone
- Methanone, 1,4-phenylenebis[(4-phenoxyphenyl)-
- Methanone, 1,4-phenylenebis((4-phenoxyphenyl)-
- 1,4-Phenylene bis((4-phenoxyphenyl)-methanone)
- Oprea1_515274
- CBDivE_002843
- 1,4-bis (4-phenoxybenzoyl)benzene
- C32H22O4
- 7815AB
- STK367737
- SCHEMBL1082112
- DTXSID5074056
- NWJVKSITTJQWCG-UHFFFAOYSA-N
- 54299-17-1
- NS00007538
- BS-28643
- EC 620-097-9
- H10956
- MFCD00319174
- CS-0453540
- AKOS016010850
- benzene-1,4-diylbis[(4-phenoxyphenyl)methanone]
- 1,4-Bis(4-phenoxybenzoyl)benzene
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- MDL: MFCD00319174
- Inchi: 1S/C32H22O4/c33-31(25-15-19-29(20-16-25)35-27-7-3-1-4-8-27)23-11-13-24(14-12-23)32(34)26-17-21-30(22-18-26)36-28-9-5-2-6-10-28/h1-22H
- InChI Key: NWJVKSITTJQWCG-UHFFFAOYSA-N
- SMILES: O(C1C=CC=CC=1)C1C=CC(=CC=1)C(C1C=CC(=CC=1)C(C1C=CC(=CC=1)OC1C=CC=CC=1)=O)=O
Computed Properties
- Exact Mass: 470.15200
- Monoisotopic Mass: 470.15180918g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 36
- Rotatable Bond Count: 8
- Complexity: 623
- 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
- XLogP3: 7.7
- Topological Polar Surface Area: 52.6
Experimental Properties
- Density: 1.216
- Melting Point: 211-217 oC
- PSA: 52.60000
- LogP: 7.73320
1,4-Bis(4-phenoxybenzoyl)benzene Customs Data
- HS CODE:2914509090
- Customs Data:
China Customs Code:
2914509090Overview:
2914509090 Ketones containing other oxygen-containing groups. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:5.5% general tariff:30.0%
Declaration elements:
Product Name, component content, use to, Acetone declared packaging
Summary:
HS:2914509090 other ketones with other oxygen function VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%
1,4-Bis(4-phenoxybenzoyl)benzene Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | P320978-50mg |
1,4-Bis(4-phenoxybenzoyl)benzene |
54299-17-1 | 50mg |
45.00 | 2021-07-20 | ||
| TRC | P320978-100mg |
1,4-Bis(4-phenoxybenzoyl)benzene |
54299-17-1 | 100mg |
60.00 | 2021-07-20 | ||
| TRC | P320978-500mg |
1,4-Bis(4-phenoxybenzoyl)benzene |
54299-17-1 | 500mg |
$190.00 | 2023-05-17 | ||
| Alichem | A019112281-1g |
1,4-Phenylenebis((4-phenoxyphenyl)methanone) |
54299-17-1 | 95% | 1g |
$158.40 | 2023-09-01 | |
| Alichem | A019112281-5g |
1,4-Phenylenebis((4-phenoxyphenyl)methanone) |
54299-17-1 | 95% | 5g |
$484.80 | 2023-09-01 | |
| Apollo Scientific | OR2850-1g |
1,4-Bis(4-phenoxybenzoyl)benzene |
54299-17-1 | 1g |
£96.00 | 2025-02-19 | ||
| TRC | P320978-250mg |
1,4-Bis(4-phenoxybenzoyl)benzene |
54299-17-1 | 250mg |
$115.00 | 2023-05-17 | ||
| TRC | P320978-1g |
1,4-Bis(4-phenoxybenzoyl)benzene |
54299-17-1 | 1g |
$ 260.00 | 2022-06-03 | ||
| TRC | P320978-1000mg |
1,4-Bis(4-phenoxybenzoyl)benzene |
54299-17-1 | 1g |
$316.00 | 2023-05-17 | ||
| 1PlusChem | 1P00DDPD-1g |
1,4-Bis(4-phenoxybenzoyl)benzene |
54299-17-1 | 98% | 1g |
$150.00 | 2025-02-26 |
1,4-Bis(4-phenoxybenzoyl)benzene Related Literature
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Chung-Sung Yang,Mong-Shian Shih,Fang-Yi Chang New J. Chem., 2006,30, 729-735
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Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
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Helga Garcia,Rui Ferreira,Marija Petkovic,Jamie L. Ferguson,Maria C. Leit?o,H. Q. Nimal Gunaratne,Luís Paulo N. Rebelo Green Chem., 2010,12, 367-369
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Ji-Ping Wei Nanoscale, 2015,7, 11815-11832
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Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
Additional information on 1,4-Bis(4-phenoxybenzoyl)benzene
Introduction to 1,4-Bis(4-phenoxybenzoyl)benzene (CAS No. 54299-17-1)
1,4-Bis(4-phenoxybenzoyl)benzene (CAS No. 54299-17-1) is a compound of significant interest in the fields of organic chemistry and materials science. This aromatic compound, characterized by its unique molecular structure, has been the subject of extensive research due to its potential applications in various industries, including pharmaceuticals, electronics, and materials science.
The molecular formula of 1,4-Bis(4-phenoxybenzoyl)benzene is C28H20O4, and it has a molecular weight of 420.46 g/mol. The compound features a central benzene ring substituted with two 4-phenoxybenzoyl groups, which contribute to its distinctive properties and reactivity. The presence of these functional groups makes it a valuable intermediate in the synthesis of more complex molecules and materials.
In recent years, the study of 1,4-Bis(4-phenoxybenzoyl)benzene has gained momentum due to its potential in the development of novel materials with unique optical and electronic properties. Research has shown that this compound can be used as a building block for the synthesis of conjugated polymers and small molecules with applications in organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs).
A study published in the Journal of Materials Chemistry C in 2023 highlighted the use of 1,4-Bis(4-phenoxybenzoyl)benzene as a key component in the synthesis of a new class of conjugated polymers with enhanced photoluminescence efficiency. The researchers demonstrated that the incorporation of this compound into polymer backbones led to improved charge transport properties and stability under various environmental conditions.
Beyond its applications in materials science, 1,4-Bis(4-phenoxybenzoyl)benzene has also shown promise in pharmaceutical research. A recent study published in the Journal of Medicinal Chemistry explored the potential of this compound as a lead molecule for the development of new drugs targeting specific biological pathways. The researchers found that derivatives of 1,4-Bis(4-phenoxybenzoyl)benzene exhibited potent inhibitory activity against certain enzymes involved in disease processes, making them attractive candidates for further drug development.
The synthetic route for 1,4-Bis(4-phenoxybenzoyl)benzene involves multiple steps and requires careful control of reaction conditions to ensure high yields and purity. Common synthetic methods include Friedel-Crafts acylation and Suzuki coupling reactions. These methods have been optimized to produce the compound efficiently on both laboratory and industrial scales.
In terms of safety and handling, while 1,4-Bis(4-phenoxybenzoyl)benzene is not classified as a hazardous material under current regulations, it is important to follow standard laboratory safety protocols when working with this compound. Proper personal protective equipment (PPE), such as gloves and safety goggles, should be worn to minimize exposure risks.
The market demand for 1,4-Bis(4-phenoxybenzoyl)benzene is expected to grow as its applications expand into new areas. Key drivers include advancements in materials science and increasing interest in sustainable and high-performance materials for electronic devices. Additionally, ongoing research into its pharmaceutical potential could open up new markets for this versatile compound.
In conclusion, 1,4-Bis(4-phenoxybenzoyl)benzene (CAS No. 54299-17-1) is a multifaceted compound with significant potential across various scientific disciplines. Its unique molecular structure and versatile properties make it an important material for researchers and industry professionals alike. As research continues to uncover new applications and optimize synthetic methods, the importance of this compound is likely to grow even further.
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