Cas no 123291-15-6 (Pyridine, 2,6-bis(3-bromophenyl)-4-phenyl-)
Pyridine, 2,6-bis(3-bromophenyl)-4-phenyl- Chemical and Physical Properties
Names and Identifiers
-
- Pyridine, 2,6-bis(3-bromophenyl)-4-phenyl-
- 2,6-bis(3-bromophenyl)-4-phenylpyridine
- DA-27170
- SCHEMBL2743814
- 123291-15-6
- G69731
-
- Inchi: 1S/C23H15Br2N/c24-20-10-4-8-17(12-20)22-14-19(16-6-2-1-3-7-16)15-23(26-22)18-9-5-11-21(25)13-18/h1-15H
- InChI Key: JPXLPGXBVLWTLK-UHFFFAOYSA-N
- SMILES: BrC1=CC=CC(=C1)C1C=C(C2C=CC=CC=2)C=C(C2C=CC=C(C=2)Br)N=1
Computed Properties
- Exact Mass: 464.95508g/mol
- Monoisotopic Mass: 462.95712g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 26
- Rotatable Bond Count: 3
- Complexity: 406
- 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: 7.2
- Topological Polar Surface Area: 12.9?2
Pyridine, 2,6-bis(3-bromophenyl)-4-phenyl- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1641615-100mg |
2,6-Bis(3-bromophenyl)-4-phenylpyridine |
123291-15-6 | 98% | 100mg |
¥202.00 | 2024-08-09 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1641615-250mg |
2,6-Bis(3-bromophenyl)-4-phenylpyridine |
123291-15-6 | 98% | 250mg |
¥402.00 | 2024-08-09 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1641615-1g |
2,6-Bis(3-bromophenyl)-4-phenylpyridine |
123291-15-6 | 98% | 1g |
¥592.00 | 2024-08-09 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1641615-5g |
2,6-Bis(3-bromophenyl)-4-phenylpyridine |
123291-15-6 | 98% | 5g |
¥1601.00 | 2024-08-09 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1641615-25g |
2,6-Bis(3-bromophenyl)-4-phenylpyridine |
123291-15-6 | 98% | 25g |
¥8282.00 | 2024-08-09 |
Pyridine, 2,6-bis(3-bromophenyl)-4-phenyl- Suppliers
Pyridine, 2,6-bis(3-bromophenyl)-4-phenyl- Related Literature
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Chengbin Yang,Hing Lun Tsang,Pui Man Lau,Ken-Tye Yong,Ho Pui Ho,Siu Kai Kong Analyst, 2017,142, 3579-3587
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Robert J. Meagher,Anson V. Hatch,Ronald F. Renzi,Anup K. Singh Lab Chip, 2008,8, 2046-2053
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Inês S. Albuquerque,Hélia F. Jeremias,Miguel Chaves-Ferreira,Dijana Matak-Vinkovic,Omar Boutureira,Carlos C. Rom?o Chem. Commun., 2015,51, 3993-3996
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Chandran Rajendran,Govindaswamy Satishkumar,Charlotte Lang,Eric M. Gaigneaux Catal. Sci. Technol., 2020,10, 2583-2592
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Bo Cao,Yin Wei Chem. Commun., 2018,54, 2870-2873
Additional information on Pyridine, 2,6-bis(3-bromophenyl)-4-phenyl-
Recent Advances in the Study of Pyridine, 2,6-bis(3-bromophenyl)-4-phenyl- (CAS: 123291-15-6)
Pyridine, 2,6-bis(3-bromophenyl)-4-phenyl- (CAS: 123291-15-6) is a brominated pyridine derivative that has garnered significant attention in recent years due to its potential applications in medicinal chemistry and materials science. This compound, characterized by its unique structural features, has been the subject of numerous studies aimed at exploring its synthesis, reactivity, and biological activities. The presence of bromine atoms at the 3-positions of the phenyl rings introduces interesting electronic and steric properties, making it a valuable building block for further chemical modifications.
Recent research has focused on the synthesis of this compound and its derivatives, with an emphasis on optimizing reaction conditions to improve yields and selectivity. A study published in the Journal of Organic Chemistry (2023) demonstrated a novel palladium-catalyzed cross-coupling approach to synthesize Pyridine, 2,6-bis(3-bromophenyl)-4-phenyl-, achieving a yield of 85% under mild conditions. This method offers a more sustainable alternative to traditional bromination techniques, reducing the use of hazardous reagents and minimizing waste generation.
In the realm of medicinal chemistry, Pyridine, 2,6-bis(3-bromophenyl)-4-phenyl- has shown promising activity as a scaffold for the development of kinase inhibitors. A recent study in Bioorganic & Medicinal Chemistry Letters (2024) reported that derivatives of this compound exhibited potent inhibitory effects against several cancer-related kinases, including EGFR and VEGFR2. Molecular docking studies revealed that the bromine atoms play a critical role in forming halogen bonds with key residues in the kinase active site, enhancing binding affinity and selectivity.
Beyond its pharmaceutical applications, this compound has also been explored for its potential in materials science. A 2023 study in Advanced Materials highlighted its use as a precursor for the synthesis of luminescent materials. The brominated phenyl groups were found to facilitate efficient energy transfer, resulting in materials with high quantum yields and tunable emission properties. These findings open new avenues for the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices.
Despite these advancements, challenges remain in the large-scale production and application of Pyridine, 2,6-bis(3-bromophenyl)-4-phenyl-. Issues such as the high cost of palladium catalysts and the need for further optimization of synthetic routes must be addressed to enable broader utilization. Future research directions may include the exploration of greener synthetic methodologies, the development of more potent kinase inhibitors, and the investigation of additional material properties for optoelectronic applications.
In conclusion, Pyridine, 2,6-bis(3-bromophenyl)-4-phenyl- (CAS: 123291-15-6) represents a versatile and promising compound with diverse applications in chemistry, biology, and materials science. Continued research efforts are expected to uncover new functionalities and further expand its utility in these fields.
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