Cas no 51339-41-4 (Methanone, (3,5-dibromophenyl)phenyl-)
Methanone, (3,5-dibromophenyl)phenyl- Chemical and Physical Properties
Names and Identifiers
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- Methanone, (3,5-dibromophenyl)phenyl-
- (3,5-dibromophenyl)-phenylmethanone
- 51339-41-4
- SCHEMBL39515
- (3,5-Dibromophenyl)(phenyl)methanone
- DTXSID90727239
-
- Inchi： 1S/C13H8Br2O/c14-11-6-10(7-12(15)8-11)13(16)9-4-2-1-3-5-9/h1-8H
- InChI Key： HSSKSBDTYLXIDN-UHFFFAOYSA-N
- SMILES： BrC1C=C(C=C(C=1)C(C1C=CC=CC=1)=O)Br
Computed Properties
- Exact Mass: 337.89414
- Monoisotopic Mass: 337.89419g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 16
- Rotatable Bond Count: 2
- Complexity: 238
- 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: 4.8
- Topological Polar Surface Area: 17.1?2
Experimental Properties
- PSA: 17.07
Methanone, (3,5-dibromophenyl)phenyl- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB606597-250mg |
(3,5-Dibromophenyl)(phenyl)methanone; . |
51339-41-4 | 250mg |
€343.80 | 2024-07-19 | ||
| abcr | AB606597-1g |
(3,5-Dibromophenyl)(phenyl)methanone; . |
51339-41-4 | 1g |
€634.10 | 2024-07-19 | ||
| abcr | AB606597-5g |
(3,5-Dibromophenyl)(phenyl)methanone; . |
51339-41-4 | 5g |
€2128.30 | 2024-07-19 |
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Methanone, (3,5-dibromophenyl)phenyl- Related Literature
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Joo Chuan Yeo,Kenry Lab Chip, 2016,16, 4082-4090
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Joseph H. Bisesi,Tara Sabo-Attwood Environ. Sci.: Nano, 2014,1, 574-583
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Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
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Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860
Additional information on Methanone, (3,5-dibromophenyl)phenyl-
Comprehensive Overview of Methanone, (3,5-dibromophenyl)phenyl- (CAS No. 51339-41-4): Properties, Applications, and Industry Insights
Methanone, (3,5-dibromophenyl)phenyl- (CAS No. 51339-41-4) is a specialized organic compound belonging to the aromatic ketone family. Its molecular structure features a phenyl group and a 3,5-dibromophenyl moiety linked via a carbonyl group, making it a valuable intermediate in synthetic chemistry. This compound has garnered attention due to its unique photophysical properties and potential applications in material science and pharmaceutical research. Researchers are increasingly exploring its role in advanced polymer formulations and organic electronics, aligning with the growing demand for sustainable materials.
The synthesis of Methanone, (3,5-dibromophenyl)phenyl- typically involves Friedel-Crafts acylation reactions, where brominated aromatic compounds are key precursors. Its high thermal stability and electron-withdrawing characteristics make it suitable for designing flame-retardant additives—a hot topic in industries seeking eco-friendly alternatives. Recent studies highlight its utility in OLED (Organic Light-Emitting Diode) technologies, where its halogenated structure enhances device efficiency. These applications resonate with current trends in green chemistry and energy-saving innovations, frequently searched topics in scientific forums.
From an analytical perspective, CAS No. 51339-41-4 is characterized by techniques like HPLC, NMR spectroscopy, and mass spectrometry. Its solubility profile (soluble in organic solvents like dichloromethane and tetrahydrofuran) is critical for laboratory handling. Safety data sheets emphasize standard precautions, such as using personal protective equipment (PPE), reflecting workplace safety trends. Notably, the compound’s low volatility reduces inhalation risks, a feature highlighted in ESG (Environmental, Social, and Governance)-focused discussions.
In the pharmaceutical sector, derivatives of Methanone, (3,5-dibromophenyl)phenyl- are investigated for bioactive molecule development. Its bromine atoms facilitate structure-activity relationship (SAR) studies, a frequent search term among medicinal chemists. Patent literature reveals its use in kinase inhibitor scaffolds, addressing demands for targeted cancer therapies. This aligns with the surge in precision medicine-related queries, showcasing the compound’s multidisciplinary relevance.
Market analysts note rising demand for CAS No. 51339-41-4 in Asia-Pacific regions, driven by electronics manufacturing growth. Regulatory compliance, such as REACH and FDA guidelines, is another trending focus, ensuring sustainable production. As industries prioritize circular economy models, recycling brominated compounds like this methanone derivative gains traction—a topic frequently explored in sustainability reports.
Future research may explore Methanone, (3,5-dibromophenyl)phenyl-’s role in carbon capture technologies or biodegradable materials, addressing climate change concerns. Collaborative efforts between academia and industry could unlock novel applications, reinforcing its position in high-value chemistry. For researchers, optimizing atom economy during synthesis remains a key challenge—a subject often queried in chemical engineering databases.
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