CAS 642-04-6

tetraphenylpyrazine

Description:

Tetraphenylpyrazine is an organic compound characterized by its unique structure, which consists of a pyrazine ring substituted with four phenyl groups. This compound is typically a crystalline solid and is known for its stability and relatively low solubility in water, making it more soluble in organic solvents. Tetraphenylpyrazine exhibits interesting electronic properties, often utilized in the field of organic electronics and photonics due to its ability to form charge-transfer complexes. It can also act as a ligand in coordination chemistry, forming complexes with various metal ions. The compound is recognized for its potential applications in materials science, particularly in the development of organic semiconductors and light-emitting devices. Additionally, tetraphenylpyrazine can undergo various chemical reactions, including oxidation and reduction, which can modify its electronic properties and reactivity. Overall, its distinctive structure and properties make tetraphenylpyrazine a subject of interest in both academic research and industrial applications.

Formula: C₂₈H₂₀N₂

InChI: InChI=1/C28H20N2/c1-5-13-21(14-6-1)25-26(22-15-7-2-8-16-22)30-28(24-19-11-4-12-20-24)27(29-25)23-17-9-3-10-18-23/h1-20H

SMILES: c1ccc(cc1)c1c(c2ccccc2)nc(c2ccccc2)c(c2ccccc2)n1

Synonyms:

• Amaron
• Benzoin-imide
• Pyrazine, 2,3,5,6-Tetraphenyl-

Oxaprozin Tetraphenylpyrazine

CAS: 642-04-6

Formula: C₂₈H₂₀N₂

Molecular weight: 384.48

Ref: ST-EA-CP-O40001

2,3,5,6-Tetraphenylpyrazine

CAS: 642-04-6

2,3,5,6-Tetraphenylpyrazine

Purity: 95%

Molecular weight: 384.48g/mol

Ref: 54-OR1050749

2,3,5,6-Tetraphenylpyrazine

Controlled Product

CAS: 642-04-6

Applications 2,3,5,6-Tetraphenylpyrazine exhibits antidiabetic activity in sucrose-loaded and streptozotocin-induced diabetic rat models.
References Goel, A., et al.: Bioorg. Med. Chem. Lett., 14, 1089 (2004)

Formula: C₂₈H₂₀N₂

Color and Shape: Neat

Molecular weight: 384.47

Ref: TR-T204561