Cas no 4837-28-9 ((4-difluoromethanesulfonylphenyl)hydrazine)

(4-Difluoromethanesulfonylphenyl)hydrazine is a specialized hydrazine derivative featuring a difluoromethanesulfonyl substituent on the phenyl ring. This compound is of interest in synthetic organic chemistry, particularly in the preparation of heterocycles and functionalized hydrazones. The electron-withdrawing sulfonyl group enhances reactivity in condensation and cyclization reactions, while the difluoromethyl moiety may influence metabolic stability in pharmaceutical applications. Its well-defined structure and high purity make it suitable for precise synthetic transformations. The compound is typically handled under controlled conditions due to its potential sensitivity. Researchers value it for its utility in constructing complex molecular architectures, particularly in medicinal chemistry and materials science.
(4-difluoromethanesulfonylphenyl)hydrazine structure
4837-28-9 structure
Product Name:(4-difluoromethanesulfonylphenyl)hydrazine
CAS No:4837-28-9
MF:C7H8F2N2O2S
MW:222.212427139282
CID:884077
Update Time:2026-04-29

(4-difluoromethanesulfonylphenyl)hydrazine Chemical and Physical Properties

Names and Identifiers

    • [4-(difluoromethylsulfonyl)phenyl]hydrazine
    • HYDRAZINE, [4-[(DIFLUOROMETHYL)SULFONYL]PHENYL]-
    • (4-((difluoromethyl)sulfonyl)phenyl)hydrazine
    • (4-Difluormethylsulfonyl-phenyl)-hydrazin
    • [4-(difluoromethane)sulfonylphenyl]hydrazine
    • {4-[(difluoromethyl)sulfonyl]phenyl}hydrazine
    • < 4-Difluormethylsulfonyl-phenyl> -hydrazin
    • AC1L6Q9D
    • AC1Q4KRF
    • AC1Q552D
    • CTK4J0786
    • NSC114906
    • p-(difluoromethylsulfonyl)phenylhydrazine
    • SureCN9702749
    • (4-difluoromethanesulfonylphenyl)hydrazine

Computed Properties

  • Exact Mass: 222.02754

Experimental Properties

  • PSA: 72.19

(4-difluoromethanesulfonylphenyl)hydrazine Pricemore >>

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Additional information on (4-difluoromethanesulfonylphenyl)hydrazine

4-Difluoromethanesulfonylphenylhydrazine (CAS No. 4837-28-9): A Comprehensive Overview

The compound 4-difluoromethanesulfonylphenylhydrazine (CAS No. 4837-28-9) is a significant chemical entity with a diverse range of applications in the fields of organic synthesis, pharmacology, and materials science. This compound, characterized by its unique structure, has garnered attention due to its potential in developing novel therapeutic agents and advanced materials. In this article, we delve into the properties, synthesis, applications, and recent advancements related to 4-difluoromethanesulfonylphenylhydrazine.

4-Difluoromethanesulfonylphenylhydrazine is an aromatic hydrazine derivative with a sulfonyl group substituted at the para position of the phenyl ring. The presence of the sulfonyl group imparts unique electronic and steric properties to the molecule, making it a versatile building block in organic chemistry. The compound's structure allows for various functionalization reactions, enabling its use in the synthesis of bioactive molecules and advanced materials.

Recent studies have highlighted the potential of sulfonamide derivatives like 4-difluoromethanesulfonylphenylhydrazine in drug discovery. Researchers have explored its role as a precursor for developing antimicrobial agents, anti-inflammatory drugs, and anticancer compounds. For instance, a 2023 study published in *Journal of Medicinal Chemistry* demonstrated that derivatives of this compound exhibit potent inhibitory activity against key enzymes involved in inflammatory pathways, suggesting its potential as a lead compound for therapeutic development.

In addition to its pharmacological applications, 4-difluoromethanesulfonylphenylhydrazine has found utility in materials science. Its ability to form stable coordination complexes has been exploited in the development of novel catalysts for organic transformations. A 2023 report in *Chemical Communications* highlighted its role as a ligand in palladium-catalyzed cross-coupling reactions, showcasing its potential in green chemistry and sustainable synthesis methods.

The synthesis of 4-difluoromethanesulfonylphenylhydrazine typically involves multi-step processes that include nucleophilic aromatic substitution and hydrazination reactions. Recent advancements in catalytic methods have enabled more efficient and environmentally friendly routes to this compound. For example, researchers have developed microwave-assisted synthesis protocols that significantly reduce reaction times while maintaining high yields.

From an analytical standpoint, 4-difluoromethanesulfonylphenylhydrazine has been employed as a reagent in various analytical techniques due to its high reactivity and selectivity. Its use in the determination of carbonyl compounds via hydrazone formation has been well-documented, with recent studies focusing on optimizing these methods for trace analysis in complex matrices.

In conclusion, 4-difluoromethanesulfonylphenylhydrazine (CAS No. 4837-28-9) stands as a pivotal compound with multifaceted applications across various scientific domains. Its unique chemical properties, coupled with recent advancements in synthesis and application methodologies, underscore its importance as a valuable tool in modern chemistry and pharmacology.

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