• 1. Evolution of dealloying induced strain in nanoporous gold crystals?
  Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
• 2. Establishing new scaling relations on two-dimensional MXenes for CO2 electroreduction?
  Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
• 3. Fatty acid positional distribution in colostrum and mature milk of women living in Inner Mongolia, North Jiangsu and Guangxi of China?
  Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
• 4. Fast-pulsing NMR techniques for the detection of weak interactions: successful natural abundance probe of hydrogen bonds in peptides?
  Amandine Altmayer-Henzien,Valérie Declerck,David J. Aitken,Ewen Lescop,Denis Merlet,Jonathan Farjon Org. Biomol. Chem., 2013,11, 7611-7615
• 5. Evolution in surface coverage of CH3NH3PbI3?XClXvia heat assisted solvent vapour treatment and their effects on photovoltaic performance of devices
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• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Organic sulfuric acids and derivatives Phenylsulfates
• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Organic sulfuric acids and derivatives Arylsulfates Phenylsulfates

(4-Methylphenyl)Oxidanesulfonic Acid: A Comprehensive Overview

(4-Methylphenyl)oxidanesulfonic acid, also known by its CAS number 3233-58-7, is a chemical compound that has garnered significant attention in various scientific and industrial fields. This compound is characterized by its unique structure, which combines a sulfonic acid group with a substituted phenyl ring. The presence of the methyl group at the para position of the phenyl ring imparts distinct chemical properties, making it a versatile molecule with potential applications in multiple domains.

The molecular structure of (4-methylphenyl)oxidanesulfonic acid consists of a benzene ring substituted with a methyl group at the fourth position and an oxidane sulfonic acid group. This arrangement not only influences its physical and chemical properties but also plays a crucial role in its reactivity and functionality. Recent studies have highlighted the importance of such structural features in determining the compound's behavior in different chemical environments.

From a physical standpoint, (4-methylphenyl)oxidanesulfonic acid exhibits specific properties that make it suitable for various applications. Its melting point, boiling point, and solubility characteristics have been extensively studied, providing valuable insights into its potential uses. For instance, its high solubility in polar solvents makes it an ideal candidate for applications in pharmaceuticals and analytical chemistry.

The synthesis of (4-methylphenyl)oxidanesulfonic acid involves several methods, each with its own advantages and limitations. One common approach is the oxidation of the corresponding sulfide precursor, which can be achieved through various oxidizing agents. Recent advancements in green chemistry have led to the development of more environmentally friendly methods for synthesizing this compound, reducing the environmental impact associated with traditional synthesis routes.

In terms of applications, (4-methylphenyl)oxidanesulfonic acid has found utility in several industries. Its use as an intermediate in pharmaceutical synthesis has been well-documented, where it serves as a building block for more complex molecules. Additionally, it has been employed in the development of advanced materials, such as polymers and composites, due to its ability to impart specific functional properties.

Recent research has also explored the potential of (4-methylphenyl)oxidanesulfonic acid in the field of electrochemistry. Studies have demonstrated its effectiveness as an electrolyte additive in lithium-ion batteries, enhancing their performance and stability. This discovery underscores the compound's versatility and opens up new avenues for its application in energy storage technologies.

The environmental impact of (4-methylphenyl)oxidanesulfonic acid has also been a topic of interest. Research into its biodegradability and toxicity has provided valuable information for its safe handling and disposal. These studies are crucial for ensuring that the compound's use aligns with sustainable practices and regulatory requirements.

In conclusion, (4-methylphenyl)oxidanesulfonic acid is a multifaceted compound with a wide range of applications across various industries. Its unique structure, combined with recent advancements in synthesis methods and application development, positions it as an important molecule in both academic research and industrial production. As further research continues to uncover new potentials, the significance of this compound is expected to grow even more pronounced.

• 72425-47-9(Sulfuric acid, ethyl 4-methylphenyl ester)
• 79812-58-1(Sulfuric acid, mono(4-methylphenyl) ester, sodium salt (1:1))
• 653605-28-8(Sulfuric acid, mono(2-methylphenyl) ester, ammonium salt)
• 69618-86-6([1,1'-Biphenyl]-3-ol,3-(hydrogen sulfate))
• 16063-85-7([1,1'-Biphenyl]-4-ol,4-(hydrogen sulfate))
• 31377-14-7(Benzonitrile,4-(sulfooxy)-)
• 26590-31-8(Benzenesulfonic acid,hydroxymethyl-)
• 17438-29-8(1,4-Benzenediol,1-(hydrogen sulfate))
• 89610-81-1(Sulfuric acid, methyl 2-methylphenyl ester)
• 85734-98-1(Phenol, 4-ethyl-, hydrogen sulfate)