Cas no 1420864-59-0 (1-(5-Bromothiophen-2-yl)sulfonylpiperazine Hydrochloride)

1-(5-Bromothiophen-2-yl)sulfonylpiperazine Hydrochloride is a high-purity synthetic compound primarily used in pharmaceutical and chemical research. Its distinctive structure, featuring a bromothiophene moiety linked to a sulfonylpiperazine group, makes it a valuable intermediate in the development of biologically active molecules. The hydrochloride salt form enhances solubility and stability, facilitating handling and storage. This compound is particularly useful in medicinal chemistry for designing kinase inhibitors and other therapeutic agents targeting signal transduction pathways. Its well-defined chemical properties and consistent quality ensure reliable performance in synthetic applications, making it a preferred choice for researchers requiring precise and reproducible results.
1-(5-Bromothiophen-2-yl)sulfonylpiperazine Hydrochloride structure
1420864-59-0 structure
Product Name:1-(5-Bromothiophen-2-yl)sulfonylpiperazine Hydrochloride
CAS No:1420864-59-0
MF:C8H12BrClN2O2S2
MW:347.680077552795
MDL:MFCD24375799
CID:2091907
PubChem ID:71636325
Update Time:2025-05-19

1-(5-Bromothiophen-2-yl)sulfonylpiperazine Hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 1-[(5-bromothiophen-2-yl)sulfonyl]pipeazine hydrochloride
    • 1-[(5-bromo-2-thienyl)sulfonyl]-Piperazine
    • 1-((5-bromothiophen-2-yl)sulfonyl)piperazine hydrochloride
    • 1-[(5-bromothiophen-2-yl)sulfonyl]piperazine hydrochloride
    • 1420864-59-0
    • EN300-30208
    • 1-((5-bromothiophen-2-yl)sulfonyl)piperazinehydrochloride
    • G19125
    • DB-237322
    • 1-(5-bromothiophen-2-yl)sulfonylpiperazine;hydrochloride
    • AKOS025980334
    • 1-(5-Bromothiophen-2-yl)sulfonylpiperazine Hydrochloride
    • MDL: MFCD24375799
    • Inchi: 1S/C8H11BrN2O2S2.ClH/c9-7-1-2-8(14-7)15(12,13)11-5-3-10-4-6-11;/h1-2,10H,3-6H2;1H
    • InChI Key: XTXRMAMXAZDFBT-UHFFFAOYSA-N
    • SMILES: BrC1=CC=C(S1)S(N1CCNCC1)(=O)=O.Cl

Computed Properties

  • Exact Mass: 345.92121g/mol
  • Monoisotopic Mass: 345.92121g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 2
  • Complexity: 311
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 86

1-(5-Bromothiophen-2-yl)sulfonylpiperazine Hydrochloride Pricemore >>

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Additional information on 1-(5-Bromothiophen-2-yl)sulfonylpiperazine Hydrochloride

1-(5-Bromothiophen-2-yl)sulfonylpiperazine Hydrochloride (CAS 1420864-59-0): A Comprehensive Overview

1-(5-Bromothiophen-2-yl)sulfonylpiperazine Hydrochloride (CAS 1420864-59-0) is a specialized sulfonylpiperazine derivative with significant potential in pharmaceutical and chemical research. This compound, characterized by its bromothiophene moiety, has garnered attention for its unique structural properties and diverse applications. Researchers and industry professionals are increasingly interested in this molecule due to its relevance in drug discovery and material science.

The molecular structure of 1-(5-Bromothiophen-2-yl)sulfonylpiperazine Hydrochloride combines a piperazine ring with a 5-bromothiophene-2-sulfonyl group, making it a valuable intermediate in organic synthesis. Its hydrochloride salt form enhances stability and solubility, which is crucial for various experimental and industrial applications. The presence of both bromine and sulfonyl functional groups allows for further chemical modifications, expanding its utility in research.

In recent years, the demand for sulfonylpiperazine derivatives like 1-(5-Bromothiophen-2-yl)sulfonylpiperazine Hydrochloride has surged, driven by their role in developing novel therapeutic agents. This compound is particularly relevant in the context of central nervous system (CNS) drug development, where piperazine-based compounds are known to exhibit bioactive properties. Researchers are exploring its potential in targeting specific receptors and enzymes, making it a hot topic in medicinal chemistry.

From a synthetic chemistry perspective, 1-(5-Bromothiophen-2-yl)sulfonylpiperazine Hydrochloride serves as a versatile building block. Its bromothiophene component enables cross-coupling reactions, such as Suzuki-Miyaura and Sonogashira couplings, which are pivotal in constructing complex molecular architectures. This adaptability aligns with the growing trend of fragment-based drug design, where small, modifiable fragments are used to develop lead compounds.

The compound's physicochemical properties, including its melting point, solubility, and stability, are critical for its application in various experimental settings. For instance, its hydrochloride salt form ensures better handling and storage, addressing common challenges in chemical research. These attributes make it a preferred choice for laboratories focusing on high-throughput screening and structure-activity relationship (SAR) studies.

Market trends indicate a rising interest in 1-(5-Bromothiophen-2-yl)sulfonylpiperazine Hydrochloride, particularly in regions with robust pharmaceutical and biotechnology sectors. Companies specializing in custom synthesis and contract research are increasingly listing this compound in their catalogs, reflecting its commercial viability. Additionally, its relevance in academic research and drug discovery pipelines underscores its importance in the scientific community.

For researchers seeking reliable sources of 1-(5-Bromothiophen-2-yl)sulfonylpiperazine Hydrochloride, it is essential to partner with reputable suppliers who provide high-purity batches. Quality control measures, such as HPLC analysis and NMR verification, are crucial to ensure consistency and reproducibility in experimental outcomes. This emphasis on quality aligns with the broader industry shift toward standardized chemical reagents.

In summary, 1-(5-Bromothiophen-2-yl)sulfonylpiperazine Hydrochloride (CAS 1420864-59-0) is a compound of significant scientific and industrial interest. Its unique structural features, combined with its applications in drug discovery and organic synthesis, position it as a valuable tool for researchers. As the demand for innovative chemical entities grows, this compound is poised to play a pivotal role in advancing both academic and industrial research endeavors.

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