Cas no 213337-42-9 (2-(Bromomethyl)quinoline hydrobromide)
2-(Bromomethyl)quinoline hydrobromide Chemical and Physical Properties
Names and Identifiers
-
- 2-(Bromomethyl)quinoline hydrobromide
- AK100719
- ANW-69988
- CTK0J7693
- KB-223845
- Quinoline, 2-(bromomethyl)-, hydrobromide
- SureCN1169842
- 2-(Bromomethyl)quinolinehydrobromide
- AKOS016001984
- SB72734
- A879152
- 2-(bromomethyl)quinoline;hydrobromide
- 2-(BROMOMETHYL)QUINOLINE HBR
- DTXSID20736056
- SCHEMBL1169842
- 2-(Bromomethyl)quinoline--hydrogen bromide (1/1)
- 213337-42-9
-
- MDL: MFCD23135774
- Inchi: 1S/C10H8BrN.BrH/c11-7-9-6-5-8-3-1-2-4-10(8)12-9;/h1-6H,7H2;1H
- InChI Key: RMCAMMGJTSBUMO-UHFFFAOYSA-N
- SMILES: BrCC1=CC=C2C=CC=CC2=N1.Br
Computed Properties
- Exact Mass: 300.91017
- Monoisotopic Mass: 300.91017g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 13
- Rotatable Bond Count: 1
- Complexity: 149
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 12.9?2
Experimental Properties
- PSA: 12.89
2-(Bromomethyl)quinoline hydrobromide Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A189007047-1g |
2-(Bromomethyl)quinoline hydrobromide |
213337-42-9 | 95% | 1g |
$545.00 | 2023-09-02 | |
| Chemenu | CM143573-1g |
2-(Bromomethyl)quinoline hydrobromide |
213337-42-9 | 95% | 1g |
$580 | 2021-08-05 | |
| TRC | B070755-50mg |
2-(Bromomethyl)quinoline hydrobromide |
213337-42-9 | 50mg |
$ 410.00 | 2022-06-07 | ||
| TRC | B070755-100mg |
2-(Bromomethyl)quinoline hydrobromide |
213337-42-9 | 100mg |
$ 680.00 | 2022-06-07 | ||
| Chemenu | CM143573-1g |
2-(Bromomethyl)quinoline hydrobromide |
213337-42-9 | 95% | 1g |
$510 | 2023-02-17 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1129813-250mg |
2-(Bromomethyl)quinoline hydrobromide |
213337-42-9 | 97% | 250mg |
¥1050.00 | 2023-11-21 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1129813-1g |
2-(Bromomethyl)quinoline hydrobromide |
213337-42-9 | 97% | 1g |
¥2437.00 | 2023-11-21 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1129813-5g |
2-(Bromomethyl)quinoline hydrobromide |
213337-42-9 | 97% | 5g |
¥6750.00 | 2023-11-21 | |
| eNovation Chemicals LLC | Y0996147-1g |
2-(Bromomethyl)quinoline hydrobromide |
213337-42-9 | 95% | 1g |
$510 | 2024-08-02 | |
| Ambeed | A762363-25g |
2-(Bromomethyl)quinoline hydrobromide |
213337-42-9 | 95+% | 25g |
$287.0 | 2024-07-28 |
2-(Bromomethyl)quinoline hydrobromide Suppliers
2-(Bromomethyl)quinoline hydrobromide Related Literature
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Peiyuan Zeng,Xiaoxiao Wang,Ming Ye,Qiuyang Ma,Jianwen Li,Wanwan Wang,Baoyou Geng,Zhen Fang RSC Adv., 2016,6, 23074-23084
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Ivor Lon?ari? Phys. Chem. Chem. Phys., 2015,17, 9436-9445
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Hongxia Li,Aikifa Raza,Qiaoyu Ge,Jin-You Lu,TieJun Zhang Soft Matter, 2020,16, 6841-6849
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Marcin Czapla,Jack Simons Phys. Chem. Chem. Phys., 2018,20, 21739-21745
-
Fereshteh Bayat Environ. Sci.: Nano, 2021,8, 367-389
Additional information on 2-(Bromomethyl)quinoline hydrobromide
2-(Bromomethyl)quinoline hydrobromide: A Comprehensive Overview
The compound 2-(Bromomethyl)quinoline hydrobromide (CAS No. 213337-42-9) is a fascinating molecule with significant potential in various scientific and industrial applications. This compound, belonging to the quinoline family, is characterized by its unique chemical structure and intriguing properties. In recent years, there has been a growing interest in exploring its synthesis, characterization, and applications across diverse fields such as pharmaceuticals, materials science, and organic synthesis.
Quinoline derivatives have long been recognized for their versatile properties due to the aromaticity of the quinoline ring and the ability to undergo various functional group transformations. The bromomethyl group attached at the 2-position of the quinoline ring introduces additional reactivity and functional versatility. This makes 2-(Bromomethyl)quinoline hydrobromide a valuable intermediate in organic synthesis, particularly in the construction of complex heterocyclic compounds.
Recent studies have highlighted the importance of hydrobromide salts in stabilizing reactive intermediates during synthesis. The hydrobromide form of 2-(Bromomethyl)quinoline not only enhances stability but also facilitates controlled reactivity during subsequent transformations. Researchers have employed this compound as a key building block in the synthesis of bioactive molecules, including potential drug candidates for treating various diseases.
In terms of synthesis, 2-(Bromomethyl)quinoline hydrobromide can be prepared via several routes, including alkylation of quinoline derivatives or bromination of appropriate precursors. The choice of synthetic pathway depends on factors such as scalability, cost-effectiveness, and the desired purity of the final product. Advanced techniques like microwave-assisted synthesis and catalytic methods have been explored to optimize the production process, ensuring higher yields and better quality control.
The physical properties of 2-(Bromomethyl)quinoline hydrobromide are equally important for its application in various fields. Its solubility characteristics, melting point, and stability under different conditions have been thoroughly investigated to determine its suitability for large-scale manufacturing and storage. These studies have provided valuable insights into its handling and transportation requirements, ensuring safe practices in industrial settings.
From an applications perspective, 2-(Bromomethyl)quinoline hydrobromide has shown promise in drug discovery programs targeting cancer, inflammation, and infectious diseases. Its ability to act as a scaffold for constructing bioactive molecules has made it a valuable asset in medicinal chemistry. Recent research has focused on modifying its structure to enhance pharmacokinetic properties such as bioavailability and metabolic stability.
In addition to pharmaceutical applications, this compound has also found use in materials science. Its incorporation into polymer systems has led to the development of novel materials with improved electronic properties. Researchers have explored its role as a precursor for synthesizing advanced materials such as conductive polymers and metal-organic frameworks (MOFs), which hold great potential for energy storage and catalysis.
The environmental impact of 2-(Bromomethyl)quinoline hydrobromide is another critical area of investigation. Studies have been conducted to assess its biodegradability and toxicity under various conditions. These findings are essential for ensuring sustainable practices in its production and use while minimizing adverse effects on ecosystems.
In conclusion, 2-(Bromomethyl)quinoline hydrobromide (CAS No. 213337-42-9) is a multifaceted compound with vast potential across multiple disciplines. Its unique chemical properties, versatile reactivity, and wide range of applications make it a subject of ongoing research interest. As advancements continue to be made in synthetic methodologies and application development, this compound is poised to play an increasingly important role in both academic research and industrial innovation.
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