Cas no 749932-70-5 (5-Bromo-1,3-dichloro-2-ethoxybenzene)
5-Bromo-1,3-dichloro-2-ethoxybenzene Chemical and Physical Properties
Names and Identifiers
-
- 5-Bromo-1,3-dichloro-2-ethoxybenzene
- 4-Bromo-2,6-dichloro-ethoxybenzene
- 4-bromo-2,6-dichlorophenyl ethyl ether
- ZZKRHZRKWYZFPH-UHFFFAOYSA-N
- DTXSID20674984
- SCHEMBL3986078
- ZEB93270
- MFCD11855952
- E90627
- AKOS015834391
- A865754
- BS-24502
- 749932-70-5
-
- MDL: MFCD11855952
- Inchi: 1S/C8H7BrCl2O/c1-2-12-8-6(10)3-5(9)4-7(8)11/h3-4H,2H2,1H3
- InChI Key: ZZKRHZRKWYZFPH-UHFFFAOYSA-N
- SMILES: BrC1C=C(C(=C(C=1)Cl)OCC)Cl
Computed Properties
- Exact Mass: 267.90600
- Monoisotopic Mass: 267.90573g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 12
- Rotatable Bond Count: 2
- Complexity: 133
- 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: 4.5
- Topological Polar Surface Area: 9.2?2
Experimental Properties
- PSA: 9.23000
- LogP: 4.15460
5-Bromo-1,3-dichloro-2-ethoxybenzene Customs Data
- HS CODE:2909309090
- Customs Data:
China Customs Code:
2909309090Overview:
2909309090 Other aromatic ethers and their halogenated derivatives\sulfonation\Nitrated derivative(Including nitrosative derivatives).Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:5.5%.general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2909309090 other aromatic ethers and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%
5-Bromo-1,3-dichloro-2-ethoxybenzene Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A019089380-5g |
5-Bromo-1,3-dichloro-2-ethoxybenzene |
749932-70-5 | 95% | 5g |
$161.12 | 2023-09-01 | |
| Alichem | A019089380-10g |
5-Bromo-1,3-dichloro-2-ethoxybenzene |
749932-70-5 | 95% | 10g |
$253.76 | 2023-09-01 | |
| TRC | B691063-100mg |
5-Bromo-1,3-dichloro-2-ethoxybenzene |
749932-70-5 | 100mg |
$ 64.00 | 2023-04-18 | ||
| TRC | B691063-250mg |
5-Bromo-1,3-dichloro-2-ethoxybenzene |
749932-70-5 | 250mg |
$ 69.00 | 2023-04-18 | ||
| TRC | B691063-500mg |
5-Bromo-1,3-dichloro-2-ethoxybenzene |
749932-70-5 | 500mg |
$ 98.00 | 2023-04-18 | ||
| TRC | B691063-1g |
5-Bromo-1,3-dichloro-2-ethoxybenzene |
749932-70-5 | 1g |
$ 138.00 | 2023-04-18 | ||
| abcr | AB273364-1 g |
5-Bromo-1,3-dichloro-2-ethoxybenzene; 97% |
749932-70-5 | 1g |
€145.40 | 2023-04-26 | ||
| abcr | AB273364-5 g |
5-Bromo-1,3-dichloro-2-ethoxybenzene; 97% |
749932-70-5 | 5g |
€395.00 | 2023-04-26 | ||
| abcr | AB273364-10 g |
5-Bromo-1,3-dichloro-2-ethoxybenzene; 97% |
749932-70-5 | 10g |
€638.30 | 2023-04-26 | ||
| abcr | AB273364-25 g |
5-Bromo-1,3-dichloro-2-ethoxybenzene; 97% |
749932-70-5 | 25g |
€1204.30 | 2023-04-26 |
5-Bromo-1,3-dichloro-2-ethoxybenzene Related Literature
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Thi Thu Tram Nguyen,Thanh Binh Nguyen Org. Biomol. Chem., 2021,19, 6015-6020
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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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Marcin Czapla,Jack Simons Phys. Chem. Chem. Phys., 2018,20, 21739-21745
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Chung-Sung Yang,Mong-Shian Shih,Fang-Yi Chang New J. Chem., 2006,30, 729-735
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Qiyuan Wu,Shangmin Xiong,Peichuan Shen,Shen Zhao,Alexander Orlov Catal. Sci. Technol., 2015,5, 2059-2064
Additional information on 5-Bromo-1,3-dichloro-2-ethoxybenzene
5-Bromo-1,3-Dichloro-2-Ethoxybenzene: A Comprehensive Overview
The compound with CAS No. 749932-70-5, commonly referred to as 5-Bromo-1,3-dichloro-2-ethoxybenzene, is a versatile organic compound with significant applications in various fields of chemistry. This compound is characterized by its unique structure, which includes a bromine atom at the 5-position, chlorine atoms at the 1 and 3 positions, and an ethoxy group at the 2-position on a benzene ring. The combination of these substituents makes it a valuable intermediate in organic synthesis and a key component in several industrial processes.
5-Bromo-1,3-dichloro-2-ethoxybenzene has been extensively studied for its role in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Recent research has highlighted its potential as a precursor for the development of novel drugs targeting specific diseases. For instance, studies have shown that derivatives of this compound exhibit promising anti-inflammatory and anti-cancer properties. These findings underscore its importance in modern drug discovery and development.
The synthesis of 5-Bromo-1,3-dichloro-2-ethoxybenzene involves a series of carefully controlled reactions. The process typically begins with the bromination of a chlorinated benzene derivative, followed by the introduction of the ethoxy group through nucleophilic substitution or other suitable methods. The precise control of reaction conditions is crucial to ensure high purity and yield of the final product. Advanced techniques such as microwave-assisted synthesis have been explored to optimize this process, making it more efficient and environmentally friendly.
In terms of applications, 5-Bromo-1,3-dichloro-2-ethoxybenzene serves as an intermediate in the production of various aromatic compounds. Its ability to undergo further functionalization makes it highly valuable in the synthesis of complex molecules. For example, it can be used to prepare biologically active compounds with specific pharmacological properties. Recent advancements in catalytic processes have further enhanced its utility in these applications.
From an environmental perspective, understanding the fate and behavior of 5-Bromo-1,3-dichloro-2-ethoxybenzene in different ecosystems is critical. Research has shown that this compound exhibits moderate biodegradability under certain conditions. However, its persistence in aquatic environments remains a concern for ecotoxicologists. Efforts are ongoing to develop sustainable methods for its disposal and recycling to minimize environmental impact.
The study of 5-Bromo-1,3-dichloro-2-ethoxybenzene has also contributed significantly to our understanding of aromatic chemistry and substitution reactions. Its reactivity patterns provide valuable insights into the design of new synthetic pathways for complex molecules. For instance, recent investigations have focused on its use as a building block for constructing heterocyclic compounds with unique electronic properties.
In conclusion, 5-Bromo-1,3-dichloro-2-ethoxybenzene is a multifaceted compound with wide-ranging applications across various disciplines. Its role as an intermediate in organic synthesis continues to be explored and expanded upon by researchers worldwide. As new technologies emerge and our understanding of its properties deepens, this compound is poised to play an even greater role in advancing chemical science.
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