Cas no 55814-63-6 (5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene)
5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene Chemical and Physical Properties
Names and Identifiers
-
- 5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene
- Benzene, 5-bromo-1,3-dichloro-2-(4-methoxyphenoxy)-
- LogP
- 55814-63-6
- SCHEMBL23663156
- DTXSID50743273
- DB-072052
-
- MDL: MFCD14706740
- Inchi: 1S/C13H9BrCl2O2/c1-17-9-2-4-10(5-3-9)18-13-11(15)6-8(14)7-12(13)16/h2-7H,1H3
- InChI Key: KGHTYPVKRDRRBL-UHFFFAOYSA-N
- SMILES: BrC1C=C(C(=C(C=1)Cl)OC1C=CC(=CC=1)OC)Cl
Computed Properties
- Exact Mass: 345.91637
- Monoisotopic Mass: 345.91630g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 18
- Rotatable Bond Count: 3
- Complexity: 247
- 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: 4.9
- Topological Polar Surface Area: 18.5?2
Experimental Properties
- Density: 1.553
- Boiling Point: 359.348°C at 760 mmHg
- Flash Point: 171.128°C
- Refractive Index: 1.602
- PSA: 18.46
5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A019089378-1g |
5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene |
55814-63-6 | 95% | 1g |
$372.00 | 2023-09-01 | |
| TRC | B071515-50mg |
5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene |
55814-63-6 | 50mg |
$ 305.00 | 2022-06-07 | ||
| TRC | B071515-100mg |
5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene |
55814-63-6 | 100mg |
$ 505.00 | 2022-06-07 | ||
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1738103-1g |
5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene |
55814-63-6 | 98% | 1g |
¥3066.00 | 2024-05-08 | |
| Crysdot LLC | CD12061181-1g |
5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene |
55814-63-6 | 95+% | 1g |
$455 | 2024-07-24 |
5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene Related Literature
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Bo Cao,Yin Wei Chem. Commun., 2018,54, 2870-2873
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2. An all-solid-state imprinted polymer-based potentiometric sensor for determination of bisphenol S?Rongning Liang,Tanji Yin,Ruiqing Yao,Wei Qin RSC Adv., 2016,6, 73308-73312
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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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Muniyandi Sankaralingam,So Hyun Jeon,Yong-Min Lee,Mi Sook Seo,Wonwoo Nam Dalton Trans., 2016,45, 376-383
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Huabin Zhang,Shaowu Du CrystEngComm, 2014,16, 4059-4068
Additional information on 5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene
5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene: A Comprehensive Overview
5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene (CAS No. 55814-63-6) is a complex organic compound with a diverse range of applications in various industries. This compound, often referred to as Bromo-Dichloro-Phenoxybenzene, has garnered significant attention due to its unique chemical properties and potential uses in pharmaceuticals, agrochemicals, and advanced materials. Recent studies have highlighted its role in enhancing the efficiency of certain chemical processes, making it a subject of interest for researchers and industry professionals alike.
The structure of 5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene is characterized by a benzene ring with substituents at specific positions. The bromine atom at position 5, chlorine atoms at positions 1 and 3, and the phenoxy group at position 2 create a highly functionalized molecule. This functionalization not only contributes to its stability but also enables it to participate in various chemical reactions, such as nucleophilic aromatic substitution and electrophilic substitution. Recent research has explored the use of this compound as an intermediate in the synthesis of bioactive molecules, particularly in the development of novel antibiotics and antiviral agents.
One of the most notable advancements involving Bromo-Dichloro-Phenoxybenzene is its application in the field of polymer chemistry. Scientists have discovered that this compound can serve as a building block for the creation of high-performance polymers with improved thermal stability and mechanical properties. These polymers have potential applications in aerospace, automotive industries, and electronic devices where durability under extreme conditions is paramount.
In addition to its industrial applications, 5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene has also been studied for its environmental impact. Researchers have investigated its biodegradation pathways and toxicity levels to aquatic organisms. Findings suggest that while the compound exhibits moderate toxicity, it can be effectively treated through advanced wastewater treatment processes, minimizing its ecological footprint.
The synthesis of Bromo-Dichloro-Phenoxybenzene involves a multi-step process that requires precise control over reaction conditions to ensure high yield and purity. Recent innovations in catalytic chemistry have enabled more efficient synthesis methods, reducing production costs and environmental impact. These advancements have made the compound more accessible for large-scale industrial use.
Looking ahead, the future of 5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene seems promising as researchers continue to uncover new applications and improve existing ones. Its role in drug discovery, polymer development, and environmental remediation underscores its versatility and importance in modern chemistry.
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