Cas no 38064-59-4 (N-(4-Hydrazinocarbonyl-phenyl)-4-methyl-benzenesulfonamide)

N-(4-Hydrazinocarbonyl-phenyl)-4-methyl-benzenesulfonamide is a sulfonamide derivative featuring a hydrazine-functionalized aromatic core, making it a versatile intermediate in organic synthesis and medicinal chemistry. Its structure combines a benzenesulfonamide moiety with a hydrazinocarbonyl group, enabling applications in the development of hydrazide-based compounds, such as inhibitors or chelating agents. The presence of the methyl group enhances stability while maintaining reactivity for further functionalization. This compound is particularly useful in the synthesis of heterocyclic frameworks and as a precursor for bioactive molecules. Its well-defined chemical properties and purity make it suitable for research in pharmaceutical and material science applications.
N-(4-Hydrazinocarbonyl-phenyl)-4-methyl-benzenesulfonamide structure
38064-59-4 structure
Product Name:N-(4-Hydrazinocarbonyl-phenyl)-4-methyl-benzenesulfonamide
CAS No:38064-59-4
MF:C14H15N3O3S
MW:305.352201700211
CID:3082370
PubChem ID:4604534
Update Time:2025-10-29

N-(4-Hydrazinocarbonyl-phenyl)-4-methyl-benzenesulfonamide Chemical and Physical Properties

Names and Identifiers

    • N-(4-Hydrazinocarbonyl-phenyl)-4-methyl-benzenesulfonamide
    • AKOS000678901
    • 38064-59-4
    • N-(4-(Hydrazinecarbonyl)phenyl)-4-methylbenzenesulfonamide
    • MDL: MFCD00593861
    • Inchi: 1S/C14H15N3O3S/c1-10-2-8-13(9-3-10)21(19,20)17-12-6-4-11(5-7-12)14(18)16-15/h2-9,17H,15H2,1H3,(H,16,18)
    • InChI Key: PPTSPBYKAFLYKA-UHFFFAOYSA-N
    • SMILES: S(C1C=CC(C)=CC=1)(NC1C=CC(C(NN)=O)=CC=1)(=O)=O

Computed Properties

  • Exact Mass: 305.083
  • Monoisotopic Mass: 305.083
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 21
  • Rotatable Bond Count: 5
  • Complexity: 445
  • 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: 1.3
  • Topological Polar Surface Area: 110A^2

N-(4-Hydrazinocarbonyl-phenyl)-4-methyl-benzenesulfonamide Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Ambeed
A171347-1g
N-(4-(Hydrazinecarbonyl)phenyl)-4-methylbenzenesulfonamide
38064-59-4 97%
1g
$294.0 2025-04-19
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1629883-5g
N-(4-(hydrazinecarbonyl)phenyl)-4-methylbenzenesulfonamide
38064-59-4 98%
5g
¥10987.00 2024-05-16

Additional information on N-(4-Hydrazinocarbonyl-phenyl)-4-methyl-benzenesulfonamide

N-(4-Hydrazinocarbonyl-phenyl)-4-methyl-benzenesulfonamide: A Comprehensive Overview

The compound with CAS No 38064-59-4, commonly referred to as N-(4-Hydrazinocarbonyl-phenyl)-4-methyl-benzenesulfonamide, is a highly specialized chemical entity that has garnered significant attention in the fields of organic chemistry, pharmacology, and materials science. This compound is characterized by its unique structure, which combines a hydrazinecarbonyl group attached to a phenyl ring and a sulfonamide group with a methyl substituent. The benzenesulfonamide moiety is particularly notable for its role in various biological and chemical applications.

Recent studies have highlighted the potential of N-(4-Hydrazinocarbonyl-phenyl)-4-methyl-benzenesulfonamide in drug discovery, where its ability to act as a bioisostere or a scaffold for constructing more complex molecules has been extensively explored. Researchers have demonstrated that this compound exhibits promising activity in inhibiting certain enzymes and receptors, making it a valuable tool in the development of novel therapeutic agents. For instance, its interaction with kinases and proteases has been investigated, revealing potential applications in oncology and inflammation-related diseases.

The synthesis of N-(4-Hydrazinocarbonyl-phenyl)-4-methyl-benzenesulfonamide involves a multi-step process that typically begins with the preparation of the hydrazinecarbonyl derivative. This is followed by coupling reactions to introduce the sulfonamide group and the methyl substituent. The optimization of these steps has been a focus of recent research, with scientists employing green chemistry principles to enhance yield and reduce environmental impact. Such advancements underscore the importance of sustainable practices in modern chemical synthesis.

In terms of structural characterization, N-(4-Hydrazinocarbonyl-phenyl)-4-methyl-benzenesulfonamide has been analyzed using advanced spectroscopic techniques such as NMR and IR spectroscopy. These studies have provided insights into its conformational flexibility and electronic properties, which are critical for understanding its reactivity and bioavailability. Furthermore, computational modeling has been employed to predict its binding affinities to various biological targets, further enhancing our understanding of its potential applications.

One of the most exciting developments involving this compound is its role in materials science. Researchers have explored its use as a building block for constructing functional polymers and nanoparticles. The benzenesulfonamide group's ability to form hydrogen bonds makes it particularly suitable for these applications, enabling the creation of materials with tailored properties such as enhanced mechanical strength or improved thermal stability.

From an environmental standpoint, the degradation pathways of N-(4-Hydrazinocarbonyl-phenyl)-4-methyl-benzenesulfonamide have also been studied to assess its ecological impact. These studies have revealed that under certain conditions, the compound undergoes hydrolysis or microbial degradation, reducing its persistence in the environment. Such findings are crucial for ensuring the responsible use and disposal of this chemical entity.

In conclusion, N-(4-Hydrazinocarbonyl-phenyl)-4-methyl-benzenesulfonamide (CAS No 38064-59-4) stands out as a versatile compound with wide-ranging applications across multiple disciplines. Its unique structure, combined with recent advancements in synthesis and characterization techniques, positions it as a key player in both academic research and industrial development. As ongoing studies continue to uncover new facets of its properties and potential uses, this compound is poised to make significant contributions to the advancement of science and technology.

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