Cas no 1520745-74-7 (Benzene, 1-bromo-3-(chloromethoxy)-)

Benzene, 1-bromo-3-(chloromethoxy)-, is a halogenated aromatic compound featuring both bromo and chloromethoxy functional groups. This structure imparts reactivity suitable for further synthetic modifications, making it valuable in organic synthesis, particularly in cross-coupling reactions and as an intermediate in pharmaceutical or agrochemical applications. The presence of both bromine and chloromethoxy substituents enhances its versatility in nucleophilic substitution and electrophilic aromatic substitution reactions. Its stability under standard conditions ensures ease of handling and storage. The compound's well-defined reactivity profile allows for precise functionalization, enabling the construction of complex molecular architectures in research and industrial settings.
Benzene, 1-bromo-3-(chloromethoxy)- structure
1520745-74-7 structure
Product Name:Benzene, 1-bromo-3-(chloromethoxy)-
CAS No:1520745-74-7
MF:C7H6BrClO
MW:221.478940486908
CID:5161140
PubChem ID:23120711
Update Time:2025-05-21

Benzene, 1-bromo-3-(chloromethoxy)- Chemical and Physical Properties

Names and Identifiers

    • Benzene, 1-bromo-3-(chloromethoxy)-
    • 1-Bromo-3-(chloromethoxy)benzene
    • Inchi: 1S/C7H6BrClO/c8-6-2-1-3-7(4-6)10-5-9/h1-4H,5H2
    • InChI Key: NNQWMSSTQYIUDE-UHFFFAOYSA-N
    • SMILES: C1(Br)=CC=CC(OCCl)=C1

Computed Properties

  • Exact Mass: 219.92906g/mol
  • Monoisotopic Mass: 219.92906g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 2
  • Complexity: 99.6
  • 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: 9.2?2

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Additional information on Benzene, 1-bromo-3-(chloromethoxy)-

Benzene, 1-bromo-3-(chloromethoxy)- (CAS No. 1520745-74-7): A Comprehensive Overview

Benzene, 1-bromo-3-(chloromethoxy)- (CAS No. 1520745-74-7) is a specialized organic compound that has garnered significant attention in the field of chemical research and industrial applications. This compound, characterized by its unique molecular structure, plays a pivotal role in various synthetic processes. Its CAS number 1520745-74-7 is often searched by researchers and industry professionals seeking detailed information about its properties and applications.

The molecular formula of 1-bromo-3-(chloromethoxy)benzene reflects its functional groups, which include a bromine atom and a chloromethoxy substituent on a benzene ring. This combination of functional groups makes it a versatile intermediate in organic synthesis. Recent trends in chemical research highlight the growing interest in halogenated benzene derivatives, particularly for their use in pharmaceuticals, agrochemicals, and advanced materials. The chloromethoxy group in this compound is especially noteworthy for its reactivity, which is leveraged in cross-coupling reactions and other synthetic transformations.

One of the most frequently asked questions about Benzene, 1-bromo-3-(chloromethoxy)- pertains to its synthesis and purification methods. Researchers often search for optimized protocols to produce this compound with high yield and purity. The compound’s stability under various conditions is another area of interest, as it impacts its storage and handling requirements. Additionally, the CAS 1520745-74-7 is commonly referenced in patents and scientific literature, underscoring its importance in innovative chemical processes.

In the context of industrial applications, 1-bromo-3-(chloromethoxy)benzene is utilized as a building block for more complex molecules. Its reactivity allows for the introduction of additional functional groups, making it a valuable tool in the development of new materials and active pharmaceutical ingredients (APIs). The demand for such intermediates has risen in tandem with advancements in green chemistry and sustainable manufacturing practices. This aligns with the broader industry shift toward environmentally friendly and efficient synthetic routes.

The safety profile of Benzene, 1-bromo-3-(chloromethoxy)- is another critical aspect explored by users. While it is not classified as a hazardous material, proper handling and disposal procedures are essential to ensure workplace safety and environmental protection. Regulatory guidelines often reference CAS No. 1520745-74-7 to provide clarity on its classification and permissible exposure limits. This information is particularly relevant for laboratories and manufacturing facilities that handle this compound regularly.

Market dynamics for 1-bromo-3-(chloromethoxy)benzene reflect its niche but growing demand. Suppliers and distributors frequently update their catalogs to include this compound, catering to the needs of academic institutions, research organizations, and industrial clients. Pricing and availability trends are closely monitored, especially by those involved in large-scale synthesis projects. The compound’s CAS 1520745-74-7 serves as a key identifier in procurement databases, ensuring accurate and efficient sourcing.

Looking ahead, the potential applications of Benzene, 1-bromo-3-(chloromethoxy)- are expected to expand further. Innovations in catalysis and synthetic methodology may unlock new uses for this compound, particularly in the development of high-performance materials and bioactive molecules. Researchers continue to explore its reactivity and compatibility with emerging technologies, such as flow chemistry and automated synthesis platforms. The compound’s chloromethoxy and bromo substituents offer a rich playground for chemical innovation.

In summary, Benzene, 1-bromo-3-(chloromethoxy)- (CAS No. 1520745-74-7) is a compound of significant scientific and industrial relevance. Its unique properties and versatile applications make it a subject of ongoing research and commercial interest. Whether you are a chemist, a procurement specialist, or a student, understanding this compound’s role in modern chemistry can provide valuable insights into the broader landscape of chemical innovation.

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