Cas no 213337-42-9 (2-(Bromomethyl)quinoline hydrobromide)

2-(Bromomethyl)quinoline hydrobromide is a versatile brominated quinoline derivative commonly employed as an intermediate in organic synthesis and pharmaceutical research. Its reactive bromomethyl group facilitates efficient functionalization, making it valuable for constructing complex heterocyclic frameworks. The hydrobromide salt form enhances stability and solubility, ensuring consistent handling in synthetic applications. This compound is particularly useful in the preparation of biologically active molecules, including potential therapeutic agents and ligands for metal coordination. High purity and well-defined reactivity contribute to its reliability in multistep syntheses. Proper storage under anhydrous conditions is recommended to maintain its integrity. Suitable for use under controlled laboratory conditions by trained professionals.
2-(Bromomethyl)quinoline hydrobromide structure
213337-42-9 structure
Product Name:2-(Bromomethyl)quinoline hydrobromide
CAS No:213337-42-9
MF:C10H9Br2N
MW:302.993160963058
MDL:MFCD23135774
CID:1038428
PubChem ID:66930346
Update Time:2025-09-27

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

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2-(Bromomethyl)quinoline hydrobromide Suppliers

Suzhou Senfeida Chemical Co., Ltd
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(CAS:213337-42-9)2-(BroMoMethyl)quinoline hydrobroMide
Order Number:sfd11801
Stock Status:in Stock
Quantity:200kg
Purity:99.9%
Pricing Information Last Updated:Friday, 19 July 2024 14:36
Price ($):discuss personally

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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Suzhou Senfeida Chemical Co., Ltd
(CAS:213337-42-9)2-(BroMoMethyl)quinoline hydrobroMide
sfd11801
Purity:99.9%
Quantity:200kg
Price ($):Inquiry
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