Cas no 57825-30-6 (1-(Bromomethyl)-4-ethylbenzene)

1-(Bromomethyl)-4-ethylbenzene is a brominated aromatic compound featuring an ethyl substituent on the benzene ring. This reagent is commonly employed in organic synthesis as an alkylating agent or intermediate for further functionalization. The bromomethyl group offers reactivity in nucleophilic substitution reactions, enabling the introduction of the 4-ethylbenzyl moiety into target molecules. Its structure makes it useful in pharmaceutical and agrochemical applications, where precise aromatic modifications are required. The compound is typically handled under inert conditions due to its sensitivity to moisture and light. Proper storage in a cool, dry environment is recommended to maintain stability. Its defined reactivity profile and purity make it a reliable choice for synthetic applications.
1-(Bromomethyl)-4-ethylbenzene structure
57825-30-6 structure
Product Name:1-(Bromomethyl)-4-ethylbenzene
CAS No:57825-30-6
MF:C9H11Br
MW:199.087641954422
MDL:MFCD09745021
CID:829702
PubChem ID:12231560
Update Time:2025-05-22

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

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.

Recommended suppliers
Zhejiang Brunova Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Zhejiang Brunova Technology Co., Ltd.
Yunnanjiuzhen
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Yunnanjiuzhen
Shandong Jing Kun Chemical Co.,Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shandong Jing Kun Chemical Co.,Ltd.
TAIXING JOXIN BIO-TEC CO.,LTD.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
TAIXING JOXIN BIO-TEC CO.,LTD.
Changzhou Guanjia Chemical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Changzhou Guanjia Chemical Co., Ltd