Cas no 330792-75-1 (N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)aniline)
N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)aniline Chemical and Physical Properties
Names and Identifiers
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- N-phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenamine
- N-phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
- XMHGCOWOUZMADX-UHFFFAOYSA-N
- MB18396
- SCHEMBL1129188
- DB-343911
- BS-48423
- EN300-12603598
- 330792-75-1
- CS-0356528
- N-phenyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
- 1-(Phenylamino)-benzene-4-boronic Acid Pinacol Ester
- N-phenyl-N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]amine
- starbld0031634
- E80459
- N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)aniline
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- Inchi: 1S/C18H22BNO2/c1-17(2)18(3,4)22-19(21-17)14-10-12-16(13-11-14)20-15-8-6-5-7-9-15/h5-13,20H,1-4H3
- InChI Key: XMHGCOWOUZMADX-UHFFFAOYSA-N
- SMILES: O1B(C2C=CC(=CC=2)NC2C=CC=CC=2)OC(C)(C)C1(C)C
Computed Properties
- Exact Mass: 295.1743591g/mol
- Monoisotopic Mass: 295.1743591g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 22
- Rotatable Bond Count: 3
- Complexity: 355
- 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: 30.5
N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)aniline Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| ChemScence | CS-0356528-5g |
N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline |
330792-75-1 | 5g |
$69.0 | 2022-04-27 | ||
| ChemScence | CS-0356528-25g |
N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline |
330792-75-1 | 25g |
$211.0 | 2022-04-27 | ||
| Aaron | AR00CN1D-10g |
N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline |
330792-75-1 | 95% | 10g |
$104.00 | 2025-02-13 | |
| Aaron | AR00CN1D-100mg |
N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline |
330792-75-1 | 95% | 100mg |
$6.00 | 2025-02-13 | |
| Aaron | AR00CN1D-250mg |
N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline |
330792-75-1 | 95% | 250mg |
$9.00 | 2025-02-13 | |
| Aaron | AR00CN1D-1g |
N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline |
330792-75-1 | 95% | 1g |
$18.00 | 2025-02-13 | |
| Aaron | AR00CN1D-5g |
N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline |
330792-75-1 | 95% | 5g |
$64.00 | 2025-02-13 | |
| Aaron | AR00CN1D-25g |
N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline |
330792-75-1 | 95% | 25g |
$200.00 | 2025-02-13 | |
| 1PlusChem | 1P00CMT1-1g |
N-phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline |
330792-75-1 | 95% | 1g |
$20.00 | 2024-05-05 | |
| 1PlusChem | 1P00CMT1-5g |
N-phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline |
330792-75-1 | 95% | 5g |
$63.00 | 2024-05-05 |
N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)aniline Related Literature
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Gaurav J. Shah,Eric P.-Y. Chiou,Ming C. Wu,Chang-Jin “CJ” Kim Lab Chip, 2009,9, 1732-1739
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Thi Thu Tram Nguyen,Thanh Binh Nguyen Org. Biomol. Chem., 2021,19, 6015-6020
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Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
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Gang Pan,Yi-jie Bao,Jie Xu,Tao Liu,Cheng Liu,Yan-yan Qiu,Xiao-jing Shi,Hui Yu,Ting-ting Jia,Xia Yuan,Ze-ting Yuan,Yi-jun Cao RSC Adv., 2016,6, 42109-42119
Additional information on N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)aniline
Comprehensive Overview of N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)aniline (CAS No. 330792-75-1)
N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)aniline, with the CAS number 330792-75-1, is a highly specialized boronic ester derivative that has garnered significant attention in the fields of organic synthesis, pharmaceutical research, and material science. This compound is particularly valued for its role as a key intermediate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. Its unique boron-containing structure makes it a versatile building block for the development of advanced drug candidates and functional materials.
The growing interest in N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)aniline is driven by its applications in targeted drug delivery systems and bioconjugation. Researchers are increasingly exploring its potential in designing proteolysis-targeting chimeras (PROTACs), a cutting-edge therapeutic approach that has become a hot topic in cancer research. Additionally, its stability and reactivity under mild conditions make it a preferred choice for high-throughput screening and combinatorial chemistry.
From an industrial perspective, CAS 330792-75-1 is often utilized in the synthesis of OLED materials and organic semiconductors, aligning with the global push toward sustainable electronics. Its compatibility with green chemistry principles has also made it a subject of interest for companies aiming to reduce environmental impact. Recent studies highlight its role in developing energy-efficient lighting solutions, a topic frequently searched in scientific databases and patent filings.
One of the most frequently asked questions about N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)aniline revolves around its synthetic scalability and purity standards. Advanced purification techniques, such as column chromatography and recrystallization, are often employed to achieve the high purity required for pharmaceutical-grade applications. Furthermore, its storage conditions and shelf life are critical considerations for laboratories and manufacturers, as improper handling can affect its reactivity and yield.
In the context of academic research, this compound is frequently cited in studies exploring boron-based therapeutics and catalysis. Its molecular structure allows for precise modifications, enabling scientists to tailor its properties for specific applications. For instance, its incorporation into fluorescent probes has opened new avenues in bioimaging and diagnostics, addressing the rising demand for non-invasive medical technologies.
The market demand for CAS 330792-75-1 is expected to grow steadily, driven by its expanding applications in personalized medicine and smart materials. As AI-driven drug discovery gains traction, the need for reliable chemical intermediates like this compound is projected to increase. Companies specializing in custom synthesis and contract research are actively investing in its production to meet the needs of biotech startups and academic institutions.
In summary, N-Phenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)aniline (330792-75-1) represents a critical component in modern chemical innovation. Its multifaceted applications, from drug development to advanced materials, underscore its importance in both scientific research and industrial processes. As the scientific community continues to uncover its potential, this compound is poised to play a pivotal role in shaping the future of molecular engineering and sustainable technology.
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