262-24-8

Basic information

• Product Name: phenoxatellurine
• Synonyms: phenoxatellurin; Phenoxatellurine
• CAS NO: 262-24-8
• Molecular Formula: C₁₂H₈OTe
• Molecular Weight: 295.7913
• Mol File: 262-24-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: phenoxatellurine(CAS DataBase Reference)
• NIST Chemistry Reference: phenoxatellurine(262-24-8)
• EPA Substance Registry System: phenoxatellurine(262-24-8)

Safety Data

• Hazardous Substances Data: 262-24-8(Hazardous Substances Data)

Usage

General Description

Phenoxatellurine is a chemical compound that contains both phenol and tellurium, making it a unique and potentially useful compound in various applications. It is known for its antioxidant properties, which can help protect cells from damage caused by free radicals. Additionally, phenoxatellurine has shown potential for use in pharmaceuticals, as it has exhibited anti-inflammatory and antibacterial properties. Its ability to scavenge free radicals and inhibit inflammation suggest that phenoxatellurine could be a promising candidate for the development of new drugs for treating conditions such as cancer, infections, and inflammatory diseases. Overall, phenoxatellurine is a versatile compound with potential therapeutic applications due to its antioxidant and anti-inflammatory properties.

Upstream product

• 31419-74-6 10,10-dichlorophenoxatellurine 
• 62167-71-9 phenoxatellurine-10,10-diacetate 
• 7732-18-5 water 
• 101-84-8 diphenylether 

Downstream Products

• 74976-35-5 2-(4-Dicyanomethylene-cyclohexa-2,5-dienylidene)-malononitrile; compound with phenoxatellurine 
• 262-20-4 phenoxathiine 
• 463-51-4 Ketene 
• 31401-51-1 phenoxatellurine-10,10-dibromide 
• 31419-74-6 10,10-dichlorophenoxatellurine 
• 3496-32-0 phenylketene 
• 262-22-6 phenoxaselenin 
• 950-47-0 phenoxathiin S,S-dioxide 

Relevant articles and documents

The reaction of phenoxatellurine with single-electron oxidizers revisited

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.