Cas no 2302-38-7 (2-bromo-4,5-dimethyl-1H-Imidazole)

2-bromo-4,5-dimethyl-1H-Imidazole structure
2302-38-7 structure
Product Name:2-bromo-4,5-dimethyl-1H-Imidazole
CAS No:2302-38-7
MF:C5H7BrN2
MW:175.026479959488
CID:1109450
PubChem ID:20156507
Update Time:2025-07-19

2-bromo-4,5-dimethyl-1H-Imidazole Chemical and Physical Properties

Names and Identifiers

    • 2-bromo-4,5-dimethyl-1H-Imidazole
    • SCHEMBL10730903
    • AT33293
    • DTXSID201300855
    • DB-163985
    • CAA30238
    • 2302-38-7
    • EN300-373501
    • MDL: MFCD21336641
    • Inchi: 1S/C5H7BrN2/c1-3-4(2)8-5(6)7-3/h1-2H3,(H,7,8)
    • InChI Key: OFXMWHDBSVVQAL-UHFFFAOYSA-N
    • SMILES: BrC1=NC(C)=C(C)N1

Computed Properties

  • Exact Mass: 173.97926g/mol
  • Monoisotopic Mass: 173.97926g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 0
  • Complexity: 86.5
  • 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: 1.9
  • Topological Polar Surface Area: 28.7?2

2-bromo-4,5-dimethyl-1H-Imidazole Pricemore >>

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Additional information on 2-bromo-4,5-dimethyl-1H-Imidazole

Comprehensive Guide to 2-Bromo-4,5-dimethyl-1H-Imidazole (CAS No. 2302-38-7): Properties, Applications, and Innovations

2-Bromo-4,5-dimethyl-1H-Imidazole (CAS No. 2302-38-7) is a versatile heterocyclic compound widely used in pharmaceutical, agrochemical, and materials science research. Its unique molecular structure, featuring a bromine-substituted imidazole ring, makes it a valuable intermediate for synthesizing bioactive molecules. This article explores its properties, applications, and recent advancements, addressing common queries like "2-bromo-4,5-dimethyl-1H-imidazole synthesis" and "CAS 2302-38-7 applications."

The compound’s chemical stability and reactivity have garnered attention in drug discovery, particularly for designing kinase inhibitors and antimicrobial agents. Researchers frequently search for "imidazole derivatives in medicinal chemistry" or "halogenated imidazoles," reflecting its relevance in targeting diseases like cancer and infections. Its role in catalysis and coordination chemistry also aligns with trends in sustainable chemistry and green synthesis.

From a structural perspective, the bromine atom at the 2-position enhances electrophilic substitution reactivity, enabling diverse functionalizations. Laboratories often inquire about "purification methods for 2-bromo-4,5-dimethyl-1H-imidazole" or "NMR spectra interpretation," underscoring its analytical importance. Recent studies highlight its utility in photocatalysis and OLED materials, addressing the growing demand for energy-efficient technologies.

In agrochemicals, 2-bromo-4,5-dimethyl-1H-imidazole serves as a precursor for herbicides and fungicides, resonating with searches like "imidazole-based crop protection." Its low environmental persistence compared to traditional halogenated compounds aligns with the "green chemistry" movement. Safety data sheets (SDS) and handling protocols are frequently requested, emphasizing proper storage (ambient conditions) and compatibility.

Innovations in scale-up synthesis and process optimization for CAS No. 2302-38-7 are trending topics, driven by cost-efficiency demands. Patents disclose novel routes using microwave-assisted reactions or flow chemistry, reducing waste and reaction times. Such advancements cater to queries like "industrial production of bromo-imidazoles."

In summary, 2-bromo-4,5-dimethyl-1H-imidazole bridges fundamental research and industrial applications, with its multidisciplinary utility ensuring sustained interest. By addressing key search terms and cutting-edge trends, this guide aims to enhance visibility while providing actionable insights for researchers and manufacturers alike.

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