Cas no 73383-95-6 (2-Bromo-N-(2-fluorophenyl)acetamide)

2-Bromo-N-(2-fluorophenyl)acetamide is a brominated acetamide derivative featuring a fluorophenyl substituent, commonly utilized as an intermediate in organic synthesis and pharmaceutical research. Its key structural attributes—the reactive bromoacetamide group and the electron-withdrawing fluorine atom—enhance its utility in nucleophilic substitution reactions and cross-coupling methodologies. The compound exhibits stability under controlled conditions and is particularly valuable in the development of fluorinated bioactive molecules. Its well-defined reactivity profile makes it suitable for applications in medicinal chemistry, where precise functionalization is required. Careful handling is advised due to its potential lachrymatory and irritant properties.
2-Bromo-N-(2-fluorophenyl)acetamide structure
73383-95-6 structure
Product Name:2-Bromo-N-(2-fluorophenyl)acetamide
CAS No:73383-95-6
MF:C8H7BrFNO
MW:232.049684762955
MDL:MFCD02974351
CID:59464
PubChem ID:3414713
Update Time:2025-05-19

2-Bromo-N-(2-fluorophenyl)acetamide Chemical and Physical Properties

Names and Identifiers

    • 2-Bromo-N-(2-fluorophenyl)acetamide
    • 2-bromo-N-(2-fluoro-phenyl)-acetamide
    • 2-bromo-N-(2-fluorophenyl)acetamide(SALTDATA: FREE)
    • AC1MPPXC
    • AG-G-90226
    • ARONIS012371
    • BBL023634
    • CTK5D7913
    • N-[(2-fluoro)phenyl]-2-bromoacetamide
    • SBB080067
    • SureCN1431346
    • SCHEMBL1431346
    • 73383-95-6
    • JMRLQUWUFLVROJ-UHFFFAOYSA-N
    • DTXSID50392265
    • AS-62290
    • CS-0186593
    • F3310-0721
    • MFCD02974351
    • AKOS000319594
    • SY079359
    • ALBB-031587
    • DB-338242
    • STL066924
    • MDL： MFCD02974351
    • Inchi： 1S/C8H7BrFNO/c9-5-8(12)11-7-4-2-1-3-6(7)10/h1-4H,5H2,(H,11,12)
    • InChI Key： JMRLQUWUFLVROJ-UHFFFAOYSA-N
    • SMILES： BrCC(NC1C=CC=CC=1F)=O

Computed Properties

  • Exact Mass: 230.97000
  • Monoisotopic Mass: 230.96950g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 3
  • Complexity: 165
  • 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: 1.8
  • Topological Polar Surface Area: 29.1?2

Experimental Properties

  • PSA: 29.10000
  • LogP: 2.23210

2-Bromo-N-(2-fluorophenyl)acetamide Customs Data

  • HS CODE：2924299090
  • Customs Data：

    China Customs Code:

    2924299090

    Overview:

    2924299090. Other cyclic amides(Including cyclic carbamates)(Including their derivatives as well as their salts). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, packing

    Summary:

    2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

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2-Bromo-N-(2-fluorophenyl)acetamide Related Literature

Related Categories

Additional information on 2-Bromo-N-(2-fluorophenyl)acetamide

2-Bromo-N-(2-fluorophenyl)acetamide (CAS No. 73383-95-6): A Comprehensive Overview of Properties and Applications

2-Bromo-N-(2-fluorophenyl)acetamide (CAS No. 73383-95-6) is a specialized organic compound with significant potential in pharmaceutical and agrochemical research. This brominated acetamide derivative features a 2-fluorophenyl group, which enhances its reactivity and makes it valuable for various synthetic applications. The compound's molecular formula is C8H7BrFNO, and it has a molecular weight of 232.05 g/mol.

One of the most searched questions about 2-Bromo-N-(2-fluorophenyl)acetamide is its role in drug discovery. Researchers frequently explore its utility as a building block for heterocyclic compounds, which are crucial in developing new antimicrobial agents and anti-inflammatory drugs. The presence of both bromine and fluorine atoms in its structure allows for selective modifications, making it a versatile intermediate in medicinal chemistry.

Another trending topic related to CAS No. 73383-95-6 is its application in agrochemical formulations. The compound's unique properties enable its use in synthesizing herbicides and pesticides, addressing the growing demand for sustainable crop protection solutions. Recent studies highlight its potential in creating environmentally friendly alternatives to traditional agrochemicals.

The physical and chemical properties of 2-Bromo-N-(2-fluorophenyl)acetamide are also a focal point for researchers. It typically appears as a white to off-white crystalline powder with a melting point range of 120–125°C. Its solubility in organic solvents like dimethyl sulfoxide (DMSO) and ethanol makes it suitable for laboratory-scale reactions. Stability under controlled conditions ensures its reliability in synthetic processes.

From an industrial perspective, the market demand for CAS No. 73383-95-6 has seen steady growth, driven by its applications in pharmaceutical intermediates and specialty chemicals. Manufacturers are increasingly optimizing production methods to meet the needs of research institutions and commercial enterprises. Quality control measures, such as HPLC and NMR analysis, are critical to ensuring the compound's purity and consistency.

In summary, 2-Bromo-N-(2-fluorophenyl)acetamide (CAS No. 73383-95-6) is a compound of high interest due to its multifaceted applications in drug development and agrochemical innovation. Its unique structural features and reactivity profile position it as a valuable tool for scientists exploring new chemical entities. As research continues to uncover its potential, this compound is likely to remain a key player in advancing synthetic and applied chemistry.

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