Cas no 57018-10-7 (2-bromo-6-chloro-4-methylphenol)
2-bromo-6-chloro-4-methylphenol Chemical and Physical Properties
Names and Identifiers
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- Phenol, 2-bromo-6-chloro-4-methyl-
- 2-bromo-6-chloro-4-methylphenol
- SCHEMBL10922054
- DTXSID80538159
- EN300-203031
- 57018-10-7
-
- MDL: MFCD22414716
- Inchi: 1S/C7H6BrClO/c1-4-2-5(8)7(10)6(9)3-4/h2-3,10H,1H3
- InChI Key: UACGFKDZXGCYIQ-UHFFFAOYSA-N
- SMILES: BrC1=C(C(=CC(C)=C1)Cl)O
Computed Properties
- Exact Mass: 219.92908
- Monoisotopic Mass: 219.92906g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 10
- Rotatable Bond Count: 0
- Complexity: 120
- 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: 3.3
- Topological Polar Surface Area: 20.2?2
Experimental Properties
- PSA: 20.23
2-bromo-6-chloro-4-methylphenol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | B673813-10mg |
2-bromo-6-chloro-4-methylphenol |
57018-10-7 | 10mg |
$ 50.00 | 2022-06-06 | ||
| TRC | B673813-50mg |
2-bromo-6-chloro-4-methylphenol |
57018-10-7 | 50mg |
$ 160.00 | 2022-06-06 | ||
| TRC | B673813-100mg |
2-bromo-6-chloro-4-methylphenol |
57018-10-7 | 100mg |
$ 230.00 | 2022-06-06 | ||
| Enamine | EN300-203031-1g |
2-bromo-6-chloro-4-methylphenol |
57018-10-7 | 95% | 1g |
$528.0 | 2023-09-16 | |
| Enamine | EN300-203031-5g |
2-bromo-6-chloro-4-methylphenol |
57018-10-7 | 95% | 5g |
$1530.0 | 2023-09-16 | |
| Enamine | EN300-203031-10g |
2-bromo-6-chloro-4-methylphenol |
57018-10-7 | 95% | 10g |
$2269.0 | 2023-09-16 | |
| Enamine | EN300-203031-0.05g |
2-bromo-6-chloro-4-methylphenol |
57018-10-7 | 95% | 0.05g |
$101.0 | 2023-09-16 | |
| Enamine | EN300-203031-0.1g |
2-bromo-6-chloro-4-methylphenol |
57018-10-7 | 95% | 0.1g |
$152.0 | 2023-09-16 | |
| Enamine | EN300-203031-0.25g |
2-bromo-6-chloro-4-methylphenol |
57018-10-7 | 95% | 0.25g |
$216.0 | 2023-09-16 | |
| Enamine | EN300-203031-0.5g |
2-bromo-6-chloro-4-methylphenol |
57018-10-7 | 95% | 0.5g |
$407.0 | 2023-09-16 |
2-bromo-6-chloro-4-methylphenol Suppliers
2-bromo-6-chloro-4-methylphenol Related Literature
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Zhiyan Chen,Nan Wu,Yaobing Wang,Bing Wang,Yingde Wang J. Mater. Chem. A, 2018,6, 516-526
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Shintaro Takata,Yoshihiro Miura Phys. Chem. Chem. Phys., 2014,16, 24784-24789
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Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
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Shun-Ze Zhan,Mian Li,Xiao-Ping Zhou,Dan Li,Seik Weng Ng RSC Adv., 2011,1, 1457-1459
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Goonay Yousefalizadeh,Shideh Ahmadi,Nicholas J. Mosey,Kevin G. Stamplecoskie Nanoscale, 2021,13, 242-252
Additional information on 2-bromo-6-chloro-4-methylphenol
Recent Advances in the Study of 2-Bromo-6-Chloro-4-Methylphenol (CAS: 57018-10-7) in Chemical and Biomedical Research
2-Bromo-6-chloro-4-methylphenol (CAS: 57018-10-7) is a halogenated phenolic compound that has garnered significant attention in recent years due to its versatile applications in chemical synthesis, pharmaceutical development, and material science. This research briefing aims to provide an up-to-date overview of the latest studies focusing on the synthesis, properties, and potential applications of this compound, particularly in the context of biomedical research.
Recent studies have highlighted the role of 2-bromo-6-chloro-4-methylphenol as a key intermediate in the synthesis of more complex organic molecules. Its unique structural features, including the presence of bromine and chlorine substituents, make it a valuable building block for the development of novel pharmaceuticals and agrochemicals. For instance, a 2023 study published in the Journal of Medicinal Chemistry demonstrated its utility in the synthesis of potential antimicrobial agents, showcasing its broad-spectrum activity against drug-resistant bacterial strains.
In addition to its synthetic applications, researchers have also explored the biological activities of 2-bromo-6-chloro-4-methylphenol. A recent investigation published in Bioorganic & Medicinal Chemistry Letters revealed its inhibitory effects on specific enzymatic pathways, suggesting potential therapeutic applications in diseases such as cancer and inflammatory disorders. The study employed advanced computational modeling and in vitro assays to elucidate the compound's mechanism of action, providing valuable insights for future drug design efforts.
Another area of interest is the environmental and toxicological profile of 2-bromo-6-chloro-4-methylphenol. A 2022 study in Environmental Science & Technology examined its degradation pathways and ecotoxicological effects, emphasizing the need for sustainable synthesis methods and proper disposal protocols. The findings underscore the importance of balancing industrial applications with environmental safety considerations.
Looking ahead, ongoing research is expected to further explore the potential of 2-bromo-6-chloro-4-methylphenol in drug discovery and material science. Collaborative efforts between chemists, biologists, and environmental scientists will be crucial in unlocking its full potential while addressing any associated challenges. This compound's unique properties and versatile applications position it as a promising candidate for future innovations in the chemical and biomedical fields.
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