Cas no 57825-30-6 (1-(Bromomethyl)-4-ethylbenzene)
1-(Bromomethyl)-4-ethylbenzene Chemical and Physical Properties
Names and Identifiers
-
- 1-(Bromomethyl)-4-ethylbenzene
- 4- ETHYLBENZYLBROMIDE
- 1-Bromomethyl-4-ethyl-benzene
- DTXSID10481563
- W17947
- EN300-80101
- 4-ethyl-benzyl bromide
- CS-0061458
- 4-ethyl benzyl bromide
- 4-ethylbenzyl bromide
- Benzene, 1-(bromomethyl)-4-ethyl-
- MFCD09745021
- AKOS009307149
- DA-16983
- YYPPFEKHXPADAV-UHFFFAOYSA-N
- SCHEMBL153348
- SB37766
- AS-60335
- 1-Bromomethyl-4-ethylbenzene
- 4-ethylbenzylbromide
- 57825-30-6
-
- MDL: MFCD09745021
- Inchi: 1S/C9H11Br/c1-2-8-3-5-9(7-10)6-4-8/h3-6H,2,7H2,1H3
- InChI Key: YYPPFEKHXPADAV-UHFFFAOYSA-N
- SMILES: BrCC1C=CC(=CC=1)CC
Computed Properties
- Exact Mass: 198.00441g/mol
- Monoisotopic Mass: 198.00441g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 10
- Rotatable Bond Count: 2
- Complexity: 82.7
- 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: 0?2
1-(Bromomethyl)-4-ethylbenzene Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| JIE DA WEI ( SHANG HAI ) YI YAO KE JI FA ZHAN Co., Ltd. | 03R0153-1g |
1-Bromomethyl-4-ethyl-benzene |
57825-30-6 | 97% | 1g |
3375.21CNY | 2021-05-08 | |
| JIE DA WEI ( SHANG HAI ) YI YAO KE JI FA ZHAN Co., Ltd. | 03R0153-5g |
1-Bromomethyl-4-ethyl-benzene |
57825-30-6 | 97% | 5g |
11787.79CNY | 2021-05-08 | |
| JIE DA WEI ( SHANG HAI ) YI YAO KE JI FA ZHAN Co., Ltd. | 03R0153-500mg |
1-Bromomethyl-4-ethyl-benzene |
57825-30-6 | 97% | 500mg |
2111.63CNY | 2021-05-08 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X48695-100mg |
1-(Bromomethyl)-4-ethylbenzene |
57825-30-6 | 95% | 100mg |
¥804.0 | 2023-09-05 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X48695-250mg |
1-(Bromomethyl)-4-ethylbenzene |
57825-30-6 | 95% | 250mg |
¥181.0 | 2024-07-18 | |
| TRC | B682218-25mg |
1-(Bromomethyl)-4-ethylbenzene |
57825-30-6 | 25mg |
$ 50.00 | 2022-06-06 | ||
| TRC | B682218-50mg |
1-(Bromomethyl)-4-ethylbenzene |
57825-30-6 | 50mg |
$ 70.00 | 2022-06-06 | ||
| TRC | B682218-250mg |
1-(Bromomethyl)-4-ethylbenzene |
57825-30-6 | 250mg |
$ 295.00 | 2022-06-06 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-IK309-100mg |
1-(Bromomethyl)-4-ethylbenzene |
57825-30-6 | 95+% | 100mg |
877CNY | 2021-05-07 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-IK309-1g |
1-(Bromomethyl)-4-ethylbenzene |
57825-30-6 | 95+% | 1g |
2922.0CNY | 2021-07-14 |
1-(Bromomethyl)-4-ethylbenzene Related Literature
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Liao Xiaoqing,Li Ruiyi,Li Zaijun,Sun Xiulan,Wang Zhouping,Liu Junkang New J. Chem., 2015,39, 5240-5248
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Tengfei Yu,Yuehan Wu,Wei Li,Bin Li RSC Adv., 2014,4, 34134-34143
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Denis V. Korchagin,Elena A. Yureva,Alexander V. Akimov,Eugenii Ya. Misochko,Gennady V. Shilov,Artem D. Talantsev,Roman B. Morgunov,Alexander A. Shakin,Sergey M. Aldoshin,Boris S. Tsukerblat Dalton Trans., 2017,46, 7540-7548
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Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
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J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
Additional information on 1-(Bromomethyl)-4-ethylbenzene
1-(Bromomethyl)-4-ethylbenzene: A Comprehensive Overview
1-(Bromomethyl)-4-ethylbenzene (CAS No. 57825-30-6) is an organic compound that has garnered significant attention in the fields of organic chemistry, materials science, and pharmaceutical research. This compound, also referred to as bromomethyl ethylbenzene, is characterized by its unique structure, which combines a bromomethyl group (-CH2Br) with an ethylbenzene moiety. The bromomethyl group imparts reactivity, making it a valuable intermediate in various synthetic processes. Recent studies have highlighted its potential applications in drug discovery and advanced materials development.
The synthesis of 1-(Bromomethyl)-4-ethylbenzene typically involves nucleophilic substitution reactions or radical-mediated processes. Researchers have explored the use of this compound as a precursor for constructing complex aromatic systems. For instance, a 2023 study published in *Organic Chemistry Frontiers* demonstrated its utility in the formation of polycyclic aromatic hydrocarbons (PAHs), which are critical components in organic electronics. The bromomethyl group serves as a versatile building block, enabling the construction of diverse molecular architectures.
In terms of applications, 1-(Bromomethyl)-4-ethylbenzene has found relevance in the development of novel pharmaceutical agents. Its ability to undergo substitution reactions facilitates the incorporation of bioactive moieties into drug candidates. A 2023 review in *Journal of Medicinal Chemistry* emphasized its role in designing kinase inhibitors, where the bromomethyl group acts as a reactive handle for further functionalization. This highlights its importance in modern drug discovery pipelines.
The compound's electronic properties have also been leveraged in materials science. Studies have shown that derivatives of 1-(Bromomethyl)-4-ethylbenzene can be used to create π-conjugated systems with tunable electronic characteristics. These systems are promising for applications in organic photovoltaics and light-emitting diodes (OLEDs). A 2023 paper in *Advanced Materials* reported the synthesis of such derivatives, showcasing their potential for high-efficiency energy conversion devices.
From an environmental perspective, understanding the fate and transport of 1-(Bromomethyl)-4-ethylbenzene is crucial for assessing its ecological impact. Recent research has focused on its degradation pathways under various environmental conditions. A 2023 study published in *Environmental Science & Technology* revealed that microbial degradation plays a significant role in reducing its persistence in aquatic systems. This knowledge is essential for developing strategies to mitigate any potential environmental risks associated with its use.
Looking ahead, the versatility of 1-(Bromomethyl)-4-ethylbenzene positions it as a key player in future chemical innovations. Its ability to serve as both a reactive intermediate and a functional building block opens up avenues for interdisciplinary research. As advancements in synthetic methodologies continue to unfold, the potential applications of this compound are expected to expand further, contributing to breakthroughs across multiple scientific domains.
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