545387-15-3

Basic information

• Product Name: 1,6,7,12-Tetra-tert-butylphenoxyperylene-3,4,9,10-tetracarboxylic dianhydride
• Synonyms: 1,6,7,1 2- tetra - t - butylphenoxy - N - N' - bis(octadecyl) - perylene - 3,4,9,10 - tetracarboxylic dianhydride
• CAS NO: 545387-15-3
• Molecular Formula: C₁₀₀H₁₃₀N₂O₈
• Molecular Weight: 1486
• Mol File: 545387-15-3.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,6,7,12-Tetra-tert-butylphenoxyperylene-3,4,9,10-tetracarboxylic dianhydride(CAS DataBase Reference)
• NIST Chemistry Reference: 1,6,7,12-Tetra-tert-butylphenoxyperylene-3,4,9,10-tetracarboxylic dianhydride(545387-15-3)
• EPA Substance Registry System: 1,6,7,12-Tetra-tert-butylphenoxyperylene-3,4,9,10-tetracarboxylic dianhydride(545387-15-3)

Safety Data

• Hazardous Substances Data: 545387-15-3(Hazardous Substances Data)

Usage

General Description

1,6,7,12-Tetra-tert-butylphenoxyperylene-3,4,9,10-tetracarboxylic dianhydride is an organic compound with a complex chemical structure. It is a type of perylene tetracarboxylic dianhydride, which is commonly used as a pigment in paints, plastics, and other industrial applications. This specific compound is modified with tert-butyl groups and a phenoxy group, which enhances its solubility and thermal stability. It is known for its vibrant red color and high thermal resistance, making it suitable for high-temperature applications. 1,6,7,12-Tetra-tert-butylphenoxyperylene-3,4,9,10-tetracarboxylic dianhydride is also used in organic electronics and optoelectronic devices for its good electron transport properties. Overall, 1,6,7,12-Tetra-tert-butylphenoxyperylene-3,4,9,10-tetracarboxylic dianhydride is a versatile chemical with various industrial and technological uses.

Upstream product

• 98-54-4 para-tert-butylphenol 
• 97097-95-5 C₆₀H₇₈Cl₄N₂O₄ 

Relevant articles and documents

Synthesis, electrochemical and optical absorption properties of new perylene-3,4:9,10-bis(dicarboximide) and perylene-3,4:9,10-bis(benzimidazole) derivatives

A series of perylene-3,4:9,10-bis(dicarboximide) (PBI) and perylene-3,4:9,10-bis(benzimidazole) (PTCBI) derivatives that are di-or tetra-substituted at the bay region by electron-donating or electron-withdrawing groups have been synthesized as soluble n-type semiconductors. Optical absorption spectroscopy and electrochemical analysis show that the nature of substitution at the bay region plays a crucial role in the modulation of the electronic properties of these PBI and PTCBI derivatives. Examination of these optical and electrochemical data in the light of energy levels identified by theoretical studies allowed a relationship between the structure and the electronic properties to be established. A relationship between the structure and electronic properties of n-type semiconductors from perylene-3,4:9,10- bis(dicarboximide) (PBI) and perylene-3,4:9,10-bis(benzimidazole) (PTCBI) series substituted at the bay region by electron-donating or electron-withdrawing groups has been established by using the complementary techniques of absorption spectroscopy, electrochemical analysis and theoretical calculations. Copyright