Cas no 731773-14-1 (2-Bromo-3-(2-methoxyphenyl)-1-propene)

2-Bromo-3-(2-methoxyphenyl)-1-propene is a brominated aromatic compound featuring a methoxyphenyl substituent and a reactive allylic bromide moiety. This structure makes it a versatile intermediate in organic synthesis, particularly for cross-coupling reactions, nucleophilic substitutions, and the preparation of more complex aromatic derivatives. The presence of the methoxy group enhances electron density, influencing reactivity in electrophilic aromatic substitutions. Its allylic bromide functionality allows for further functionalization, making it valuable in pharmaceutical and agrochemical research. The compound is typically handled under inert conditions due to its sensitivity to moisture and light. Proper storage and handling ensure stability and optimal performance in synthetic applications.
2-Bromo-3-(2-methoxyphenyl)-1-propene structure
731773-14-1 structure
Product Name:2-Bromo-3-(2-methoxyphenyl)-1-propene
CAS No:731773-14-1
MF:C10H11BrO
MW:227.097742319107
MDL:MFCD07698640
CID:879299
PubChem ID:24721828
Update Time:2025-10-24

2-Bromo-3-(2-methoxyphenyl)-1-propene Chemical and Physical Properties

Names and Identifiers

    • 1-(2-bromoprop-2-enyl)-2-methoxybenzene
    • 2-BROMO-3-(2-METHOXYPHENYL)-1-PROPENE
    • 731773-14-1
    • 1-(2-Bromoprop-2-en-1-yl)-2-methoxybenzene
    • DTXSID10641180
    • MFCD07698640
    • AKOS016016813
    • 2-Bromo-3-(2-methoxyphenyl)-1-propene
    • MDL: MFCD07698640
    • Inchi: 1S/C10H11BrO/c1-8(11)7-9-5-3-4-6-10(9)12-2/h3-6H,1,7H2,2H3
    • InChI Key: MKMZHQBTAFKEFC-UHFFFAOYSA-N
    • SMILES: BrC(=C)CC1C=CC=CC=1OC

Computed Properties

  • Exact Mass: 225.99900
  • Monoisotopic Mass: 225.99933g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 3
  • Complexity: 156
  • 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: 3.9
  • Topological Polar Surface Area: 9.2?2

Experimental Properties

  • Density: 1.329
  • Boiling Point: 259.8°C at 760 mmHg
  • Flash Point: 102.9°C
  • Refractive Index: 1.549
  • PSA: 9.23000
  • LogP: 3.14630

2-Bromo-3-(2-methoxyphenyl)-1-propene Customs Data

  • HS CODE:2909309090
  • Customs Data:

    China Customs Code:

    2909309090

    Overview:

    2909309090 Other aromatic ethers and their halogenated derivatives\sulfonation\Nitrated derivative(Including nitrosative derivatives).Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:5.5%.general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2909309090 other aromatic ethers and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

2-Bromo-3-(2-methoxyphenyl)-1-propene Pricemore >>

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2-Bromo-3-(2-methoxyphenyl)-1-propene Related Literature

Additional information on 2-Bromo-3-(2-methoxyphenyl)-1-propene

Comprehensive Overview of 2-Bromo-3-(2-methoxyphenyl)-1-propene (CAS No. 731773-14-1)

2-Bromo-3-(2-methoxyphenyl)-1-propene, identified by its CAS No. 731773-14-1, is a specialized organic compound widely utilized in pharmaceutical and agrochemical research. This compound features a unique molecular structure combining a bromo substituent with a methoxyphenyl group, making it a valuable intermediate in synthetic chemistry. Researchers and industries are increasingly interested in this compound due to its potential applications in drug discovery and material science.

One of the most searched questions regarding 2-Bromo-3-(2-methoxyphenyl)-1-propene is its role in cross-coupling reactions, particularly in Suzuki-Miyaura and Heck reactions. These reactions are pivotal in constructing complex organic frameworks, a topic highly relevant in modern green chemistry and sustainable synthesis. The compound’s bromine moiety acts as a reactive handle, enabling efficient bond formation under mild conditions, which aligns with the growing demand for eco-friendly chemical processes.

Another trending topic tied to CAS No. 731773-14-1 is its potential in medicinal chemistry. The methoxyphenyl group is a common pharmacophore found in bioactive molecules, sparking interest in its use for developing anti-inflammatory and antioxidant agents. Recent studies highlight its utility in designing small-molecule inhibitors, addressing current challenges in drug resistance and targeted therapies.

From a technical perspective, the synthesis of 2-Bromo-3-(2-methoxyphenyl)-1-propene involves electrophilic aromatic substitution and allylic bromination, processes frequently discussed in academic forums. Optimizing these methods to achieve higher yields and selectivity remains a key focus, especially for industrial-scale production. Users often search for synthetic protocols and spectroscopic data (e.g., NMR, IR) to validate purity, underscoring the need for reliable analytical references.

The compound’s stability under various conditions is another frequently queried aspect. While it is generally stable at room temperature, precautions such as storage in anhydrous environments and protection from UV light are recommended to prevent degradation. This aligns with broader industry trends emphasizing chemical storage best practices and safety compliance.

In material science, 731773-14-1 has garnered attention for its potential in organic electronics. Its conjugated system and electron-donating methoxy group make it a candidate for organic semiconductors and light-emitting diodes (OLEDs). Researchers exploring next-generation optoelectronic materials often investigate such derivatives, reflecting the intersection of chemistry and advanced technology.

To conclude, 2-Bromo-3-(2-methoxyphenyl)-1-propene (CAS No. 731773-14-1) is a versatile building block with multifaceted applications. Its relevance in pharmaceutical synthesis, catalysis, and material innovation ensures sustained interest across scientific disciplines. As the demand for tailored organic compounds grows, this compound will likely remain a focal point in both academic and industrial research.

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