262-24-8 Usage
Uses
Used in Pharmaceutical Applications:
Phenoxatellurine is used as a potential therapeutic agent for its antioxidant properties, which can help in the development of new drugs for treating conditions such as cancer, infections, and inflammatory diseases. Its ability to scavenge free radicals and inhibit inflammation makes it a promising candidate for pharmaceutical research and development.
Used in Antioxidant Formulations:
In the health and wellness industry, phenoxatellurine is used as an antioxidant ingredient in dietary supplements and skincare products. Its capacity to neutralize free radicals contributes to the protection of cells from oxidative stress, which is associated with aging and various health issues.
Used in Antibacterial Agents:
Phenoxatellurine is utilized as an antibacterial component in various applications, such as in the development of new antibiotics or as a component in disinfectants and sanitizers. Its antimicrobial properties can help combat bacterial infections and contribute to improved hygiene and public health.
Used in Inflammatory Disease Treatment:
In the medical field, phenoxatellurine is used as an anti-inflammatory agent for the treatment of inflammatory diseases. Its potential to reduce inflammation and associated pain could lead to the development of new treatments for conditions such as arthritis, asthma, and other inflammatory disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 262-24-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,6 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 262-24:
(5*2)+(4*6)+(3*2)+(2*2)+(1*4)=48
48 % 10 = 8
So 262-24-8 is a valid CAS Registry Number.
262-24-8Relevant academic research and scientific papers
Mostaghimi, Farzin,Lork, Enno,Hong, Intek,Roemmele, Tracey L.,Boeré, René T.,Mebs, Stefan,Beckmann, Jens
, p. 12754 - 12766 (2019)
The reaction of phenoxatellurine (PT) with the known single-electron oxidizers AlCl3/CH2Cl2, [NO][SbF6] and [NO][BF4] provided the diamagnetic products [(PT)CH2Cl][AlCl4] (1), [PT2][SbF6]2 (2) and [PT3][BF4]2 (3), respectively, which were fully characterized by X-ray crystallography. The dications [PT2]2+ and [PT3]2+ present in 2 and 3 can be regarded as dimers of the elusive radical cation [PT]+ or as adduct between this dimer and neutral PT, respectively. The stacking between the aromatic layers of [PT2]2+ and [PT3]2+ can be best described using the pancake bonding (PB) model. The computational analysis uncovers the essential role of London dispersion effects for the stacking process and reveals the Te-Te interactions to be dominated by non-covalent bonding. The results are compared with those of the related thianthrene (TA) system.
Anion Chelation via Double Chalcogen Bonding: The Case of a Bis-Telluronium Dication and Its Application in Electrophilic Catalysis via Metal-Chloride Bond Activation
Gabba?, Fran?ois P.,Zhou, Benyu
supporting information, p. 8625 - 8630 (2021/06/28)
Telluronium cations have long been known to engage their counteranions via secondary interactions. Yet, this property has rarely been exploited for anion binding. Motivated by such an application, we have now synthesized a bis-Telluronium dication ([3]2+)
