Cas no 4837-28-9 ((4-difluoromethanesulfonylphenyl)hydrazine)
(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 >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | D591758-25mg |
(4-difluoromethanesulfonylphenyl)hydrazine |
4837-28-9 | 25mg |
$ 70.00 | 2022-06-05 | ||
| TRC | D591758-50mg |
(4-difluoromethanesulfonylphenyl)hydrazine |
4837-28-9 | 50mg |
$ 95.00 | 2022-06-05 | ||
| TRC | D591758-250mg |
(4-difluoromethanesulfonylphenyl)hydrazine |
4837-28-9 | 250mg |
$ 365.00 | 2022-06-05 | ||
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1112949-100mg |
(4-Difluoromethanesulfonylphenyl)hydrazine |
4837-28-9 | 97% | 100mg |
¥1733.00 | 2024-05-12 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1112949-250mg |
(4-Difluoromethanesulfonylphenyl)hydrazine |
4837-28-9 | 97% | 250mg |
¥2086.00 | 2024-05-12 | |
| Enamine | EN300-65327-0.05g |
(4-difluoromethanesulfonylphenyl)hydrazine |
4837-28-9 | 95% | 0.05g |
$88.0 | 2023-02-13 | |
| Enamine | EN300-65327-0.1g |
(4-difluoromethanesulfonylphenyl)hydrazine |
4837-28-9 | 95% | 0.1g |
$132.0 | 2023-02-13 | |
| Enamine | EN300-65327-0.25g |
(4-difluoromethanesulfonylphenyl)hydrazine |
4837-28-9 | 95% | 0.25g |
$188.0 | 2023-02-13 | |
| Enamine | EN300-65327-0.5g |
(4-difluoromethanesulfonylphenyl)hydrazine |
4837-28-9 | 95% | 0.5g |
$353.0 | 2023-02-13 | |
| Enamine | EN300-65327-1.0g |
(4-difluoromethanesulfonylphenyl)hydrazine |
4837-28-9 | 95% | 1.0g |
$470.0 | 2023-02-13 |
(4-difluoromethanesulfonylphenyl)hydrazine Related Literature
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1. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198
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Matthew J. Gaunt,Jinquan Yu,Jonathan B. Spencer Chem. Commun., 2001, 1844-1845
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Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
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Jacob S. Jordan,Evan R. Williams Analyst, 2021,146, 2617-2625
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Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
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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