Cas no 2065-04-5 (N-3-(2-bromoacetyl)phenylmethanesulfonamide)

N-3-(2-bromoacetyl)phenylmethanesulfonamide is a bromoacetyl-substituted sulfonamide derivative with applications in organic synthesis and pharmaceutical research. Its key structural features include a reactive bromoacetyl group, which facilitates selective alkylation or conjugation reactions, and a phenylmethanesulfonamide moiety that enhances stability and solubility. This compound is particularly useful as an intermediate in the development of biologically active molecules, such as enzyme inhibitors or targeted therapeutics. Its well-defined reactivity profile and compatibility with various reaction conditions make it a valuable reagent for medicinal chemistry and drug discovery. The product is typically supplied in high purity, ensuring consistent performance in synthetic applications.
N-3-(2-bromoacetyl)phenylmethanesulfonamide structure
2065-04-5 structure
Product Name:N-3-(2-bromoacetyl)phenylmethanesulfonamide
CAS No:2065-04-5
MF:C9H10BrNO3S
MW:292.149600505829
MDL:MFCD11052994
CID:1395157
PubChem ID:11346858
Update Time:2025-11-05

N-3-(2-bromoacetyl)phenylmethanesulfonamide Chemical and Physical Properties

Names and Identifiers

    • Methanesulfonamide, N-[3-(bromoacetyl)phenyl]-
    • N-3-(2-bromoacetyl)phenylmethanesulfonamide
    • 2-bromo-1-[3-(methylsulfonyl)aminophenyl]ethanone
    • 2065-04-5
    • N-[3-(2-Bromo-acetyl)-phenyl]-methanesulfonamide
    • SCHEMBL1120803
    • 3'-(2-bromoacetyl)methanesulfonanilide
    • CS-0116993
    • 2-bromo-1-[3-[(methylsulfonyl)amino]phenyl]ethanone
    • EN300-9493480
    • N-(3-(2-Bromoacetyl)phenyl)methanesulfonamide
    • CPSLFLKTEZYTER-UHFFFAOYSA-N
    • N-[3-(2-bromoacetyl)phenyl]methanesulfonamide
    • G64848
    • starbld0044777
    • AKOS000278455
    • MDL: MFCD11052994
    • Inchi: 1S/C9H10BrNO3S/c1-15(13,14)11-8-4-2-3-7(5-8)9(12)6-10/h2-5,11H,6H2,1H3
    • InChI Key: CPSLFLKTEZYTER-UHFFFAOYSA-N
    • SMILES: BrCC(C1=CC=CC(=C1)NS(C)(=O)=O)=O

Computed Properties

  • Exact Mass: 290.9565
  • Monoisotopic Mass: 290.95648g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 4
  • Complexity: 323
  • 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: 2.4
  • Topological Polar Surface Area: 71.6?2

Experimental Properties

  • PSA: 63.24

N-3-(2-bromoacetyl)phenylmethanesulfonamide Pricemore >>

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Additional information on N-3-(2-bromoacetyl)phenylmethanesulfonamide

Market Research and Analysis of N-3-(2-bromoacetyl)phenylmethanesulfonamide in the Chemical-Biomedical Field

The compound N-3-(2-bromoacetyl)phenylmethanesulfonamide, identified by the CAS registry number 2065-04-5, has garnered significant attention in the chemical-biomedical industry due to its unique properties and potential applications. This research brief aims to provide an in-depth analysis of the latest developments, market demands, and future prospects of this compound within the chemical-biomedical field.

The compound N-3-(2-bromoacetyl)phenylmethanesulfonamide is a derivative of methanesulfonamide, which is widely used in organic synthesis and drug development. Its structure incorporates a bromoacetyl group, which enhances its reactivity and bioavailability. Recent studies have highlighted its potential as a precursor for synthesizing bioactive molecules, particularly in the fields of oncology and neurodegenerative diseases.

Market demand for N-3-(2-bromoacetyl)phenylmethanesulfonamide has been driven by its role as an intermediate in drug discovery processes. The increasing focus on personalized medicine and the development of targeted therapies have further amplified its significance. According to industry reports, global suppliers are actively scaling up production to meet the rising demand from pharmaceutical companies and research institutions.

The purpose of this research is to evaluate the current market landscape of N-3-(2-bromoacetyl)phenylmethanesulfonamide, identify key drivers and challenges, and provide insights into future trends. This analysis is based on a comprehensive review of academic publications, industry reports, and supplier data.

To conduct this study, we employed a multi-faceted approach that included keyword searches in scientific databases (such as PubMed and ScienceDirect), analysis of market trends using tools like Statista and IBISWorld, and direct outreach to suppliers for real-time data. The results were synthesized to provide a holistic view of the compound's market dynamics.

The findings reveal that N-3-(2-bromoacetyl)phenylmethanesulfonamide is increasingly being utilized in preclinical studies for its ability to modulate key cellular pathways. Its role as an intermediate in the synthesis of kinase inhibitors has been particularly noteworthy. Additionally, its application in combinatorial chemistry has expanded its utility across diverse therapeutic areas.

In terms of supply chain dynamics, several global chemical manufacturers have established dedicated production lines for this compound. The Asia-Pacific region has emerged as a major production hub due to favorable regulatory environments and lower production costs. However, challenges such as raw material shortages and stringent regulatory requirements remain significant barriers to scaling up production.

In conclusion, N-3-(2-bromoacetyl)phenylmethanesulfonamide holds immense potential in the chemical-biomedical field, driven by its versatility in drug discovery applications. As the demand for bioactive intermediates continues to grow, it is anticipated that this compound will play an increasingly critical role in advancing therapeutic innovations.

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