Cas no 29604-75-9 (2,4-Dibromo-1-chlorobenzene)
2,4-Dibromo-1-chlorobenzene Chemical and Physical Properties
Names and Identifiers
-
- 2,4-Dibromo-1-chlorobenzene
- 1-Chloro-2,4-dibromobenzene
- Benzene,2,4-dibromo-1-chloro-
- EN300-1915598
- FT-0745579
- N12666
- A854269
- 29604-75-9
- Benzene, 2,4-dibromo-1-chloro-
- CS-0036747
- 2, 4-dibromo-1-chlorobenzene
- DTXSID00554674
- FS-6530
- SCHEMBL11318966
- AKOS016845242
- DA-07242
- MFCD11845901
-
- MDL: MFCD11845901
- Inchi: 1S/C6H3Br2Cl/c7-4-1-2-6(9)5(8)3-4/h1-3H
- InChI Key: IJZDMPWKIBVVCQ-UHFFFAOYSA-N
- SMILES: BrC1C(=CC=C(C=1)Br)Cl
Computed Properties
- Exact Mass: 267.82899
- Monoisotopic Mass: 267.82900g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 9
- Rotatable Bond Count: 0
- Complexity: 97.1
- 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: 3.9
- Topological Polar Surface Area: 0?2
Experimental Properties
- Density: 2.021±0.06 g/cm3 (20 oC 760 Torr),
- Melting Point: 27°C
- Boiling Point: 256.1±20.0 oC (760 Torr),
- Flash Point: 118.5±11.9 oC,
- Refractive Index: 1.5300 (estimate)
- Solubility: Insuluble (7.6E-3 g/L) (25 oC),
- PSA: 0
2,4-Dibromo-1-chlorobenzene Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 037509-1g |
1-Chloro-2,4-dibromobenzene |
29604-75-9 | 95% | 1g |
£247.00 | 2022-03-01 | |
| Alichem | A013026414-5g |
2,4-Dibromo-1-chlorobenzene |
29604-75-9 | 95% | 5g |
$1185.60 | 2023-09-02 | |
| eNovation Chemicals LLC | Y1254264-25g |
Benzene, 2,4-dibromo-1-chloro- |
29604-75-9 | 97% | 25g |
$120 | 2024-06-07 | |
| Enamine | EN300-1915598-1g |
2,4-dibromo-1-chlorobenzene |
29604-75-9 | 1g |
$342.0 | 2023-09-17 | ||
| Enamine | EN300-1915598-5g |
2,4-dibromo-1-chlorobenzene |
29604-75-9 | 5g |
$991.0 | 2023-09-17 | ||
| Enamine | EN300-1915598-10g |
2,4-dibromo-1-chlorobenzene |
29604-75-9 | 10g |
$1471.0 | 2023-09-17 | ||
| Enamine | EN300-1915598-0.05g |
2,4-dibromo-1-chlorobenzene |
29604-75-9 | 0.05g |
$287.0 | 2023-09-17 | ||
| Enamine | EN300-1915598-0.1g |
2,4-dibromo-1-chlorobenzene |
29604-75-9 | 0.1g |
$301.0 | 2023-09-17 | ||
| Enamine | EN300-1915598-0.25g |
2,4-dibromo-1-chlorobenzene |
29604-75-9 | 0.25g |
$315.0 | 2023-09-17 | ||
| Enamine | EN300-1915598-0.5g |
2,4-dibromo-1-chlorobenzene |
29604-75-9 | 0.5g |
$328.0 | 2023-09-17 |
2,4-Dibromo-1-chlorobenzene Suppliers
2,4-Dibromo-1-chlorobenzene Related Literature
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Supaporn Sawadjoon,Joseph S. M. Samec Org. Biomol. Chem., 2011,9, 2548-2554
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Li-Hua Gan,Rui Wu,Jian-Lei Tian,Patrick W. Fowler Phys. Chem. Chem. Phys., 2017,19, 419-425
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José M. Rivera,Mariana Martín-Hidalgo,Jean C. Rivera-Ríos Org. Biomol. Chem., 2012,10, 7562-7565
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Xiang Liu,Qian Sun,A. B. Djuri?i?,Maohai Xie,Baohu Dai,Jinyao Tang,Charles Surya,Changzhong Liao,Kaimin Shih RSC Adv., 2015,5, 100783-100789
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Raheleh Torabi,Hedayatollah Ghourchian,Massoud Amanlou Org. Biomol. Chem., 2016,14, 8141-8153
Additional information on 2,4-Dibromo-1-chlorobenzene
Introduction to 2,4-Dibromo-1-Chlorobenzene (CAS No. 29604-75-9)
2,4-Dibromo-1-chlorobenzene, also known by its CAS number 29604-75-9, is a brominated aromatic compound with a unique structure that makes it valuable in various chemical applications. This compound is characterized by the presence of bromine atoms at the 2 and 4 positions of the benzene ring, along with a chlorine atom at the 1 position. The combination of these halogens imparts distinctive chemical properties, making it a subject of interest in both academic and industrial research.
The synthesis of 2,4-dibromo-1-chlorobenzene typically involves electrophilic substitution reactions on benzene derivatives. Recent studies have explored more efficient methods to synthesize this compound, leveraging advanced catalytic systems and green chemistry principles. For instance, researchers have reported the use of microwave-assisted synthesis to enhance reaction rates and reduce energy consumption during the bromination process.
In terms of physical properties, 2,4-dibromo-1-chlorobenzene is a crystalline solid with a melting point of approximately 85°C. Its solubility in organic solvents such as dichloromethane and chloroform makes it suitable for various chemical transformations. The compound exhibits moderate stability under normal conditions but can undergo decomposition under high temperatures or in the presence of strong oxidizing agents.
The chemical structure of 2,4-dibromo-1-chlorobenzene plays a crucial role in its reactivity. The presence of electron-withdrawing groups (bromine and chlorine) activates the benzene ring towards further substitution reactions. This property has been exploited in the development of novel materials, including polymeric compounds with enhanced thermal stability and mechanical strength.
Recent research has highlighted the potential of 2,4-dibromo-1-chlorobenzene as an intermediate in the synthesis of biologically active molecules. For example, studies have demonstrated its use in the preparation of antiviral agents and anticancer drugs. The compound's ability to undergo nucleophilic aromatic substitution reactions has been particularly valuable in these applications.
In environmental science, 2,4-dibromo-1-chlorobenzene has been studied for its behavior in aqueous systems and its potential impact on aquatic ecosystems. Researchers have investigated its degradation pathways under UV light and microbial action, providing insights into its environmental fate and toxicity.
The application of 2,4-dibromo-1-chlorobenzene extends to the electronics industry, where it serves as a precursor for the synthesis of advanced materials such as liquid crystal polymers and dielectric resins. Its unique electronic properties make it an attractive candidate for use in high-performance electronic devices.
In conclusion, 2,4-dibromo-1-chlorobenzene (CAS No. 29604-75-9) is a versatile compound with a wide range of applications across different fields. Its chemical structure and reactivity continue to be subjects of extensive research, driven by the demand for innovative materials and sustainable chemical processes.
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