57103-21-6

Basic information

• Product Name: 3,6-DIIODO-9-PHENYL-9H-CARBAZOLE
• Synonyms: 3,6-DIIODO-9-PHENYL-9H-CARBAZOLE;3,6-Diiodo-9-phenylcarbazole;9H-Carbazole,3,6-diiodo-9-phenyl
• CAS NO: 57103-21-6
• Molecular Formula: C₁₈H₁₁I₂N
• Molecular Weight: 495.10
• Mol File: 57103-21-6.mol
• Article Data: 15

Chemical Properties

• Melting Point: 181.0 to 185.0 °C
• Boiling Point: 540.837 °C at 760 mmHg
• Flash Point: 280.888 °C
• Appearance: white to pink yellow powder or crystals
• Density: 1.947 g/cm³
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• Solubility: slightly sol. in dichloromethane
• CAS DataBase Reference: 3,6-DIIODO-9-PHENYL-9H-CARBAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,6-DIIODO-9-PHENYL-9H-CARBAZOLE(57103-21-6)
• EPA Substance Registry System: 3,6-DIIODO-9-PHENYL-9H-CARBAZOLE(57103-21-6)

Safety Data

• Hazardous Substances Data: 57103-21-6(Hazardous Substances Data)

Usage

General Description

3,6-Diiodo-9-phenyl-9H-carbazole, also known as DPBC, is a chemical compound with the molecular formula C24H14I2N. It is a derivative of carbazole, a tricyclic aromatic hydrocarbon, and is characterized by the presence of two iodine atoms at positions 3 and 6 of the carbazole ring. DPBC has been studied and used in various applications, such as in the synthesis of organic semiconductors and as a component in photovoltaic devices. Its unique structure and properties make it a valuable building block for the development of advanced materials for optoelectronic and electronic devices. Additionally, DPBC has attracted attention for its potential use in medicinal chemistry due to its interesting biological activities.

Upstream product

• 1150-62-5 N-phenylcarbazole 
• 57103-20-5 3,6-dibromo-9-phenyl-9H-carbazole 
• 86-74-8 9H-carbazole 
• 591-50-4 iodobenzene 

Downstream Products

• 180507-24-8 N-phenylcarbazole-3,6-bis-[N,N,N'-tris-(trimethylsilyl)-carboxamidine] 
• 1092807-67-4 C₅₀H₄₃N₃O₄ 
• 1026033-48-6 3-(6-iodo-9-phenyl)carbazolyldiphenylamine 
• 211685-96-0 3,6-di(9H-carbazol-9-yl)-9-phenyl-9H-carbazole 
• 1401068-29-8 C₃₁H₂₀N₄ 
• 1401068-30-1 C₃₁H₁₉IN₄ 
• 1401067-94-4 C₄₄H₂₇N₇ 
• 918137-86-7 (9,9'-diphenyl-9H,9'H-[3,3'-biscarbazol]-6-yl)boronic acid 

Relevant articles and documents

Synthesis, crystal structures, and nonlinear optic and thermal properties of two diiodocarbazole derivatives

Two 3,6-diiodocarbazole derivatives were prepared from the iodination of the corresponding phenylcarbazole. 3,6-Diiodo-9-phenylcarbazole crystallises in the chiral space group P21 and shows good second-harmonic generation effects. Thermogravime

Crystal structure of type-A 3,6-diiodo-N-phenylcarbazole and preparation method of crystal structure

The invention discloses a crystal structure of type-A 3,6-diiodo-N-phenylcarbazole and a preparation method of the crystal structure. The preparation method of the crystal structure comprises steps as follows: 0.1 g of 3,6-diiodo-N-phenylcarbazole is weig

N-PHENYL TRISCARBAZOLE

The present invention relates to a novel triscarbazole compound having substituent on N-phenyl, which can be represented by Formula (I). wherein R1 is selected from the group consisting of hydrogen, halogen or alkyl or alkoxy group having 1 to 20 carbon atoms wherein at least one hydrogen atom is optionally replaced by halogen; RA, RB, RC, RD and RE are any of substituents other than hydrogen wherein at least two of R1 and RA may further form a fused ring; and i, j, k, l and m are same or different at each occurrence and represent an integer from 0 to 4, with the proviso that when R1 is hydrogen, i is not 0. By introduction of the substituent on N-phenyl, the device efficiency, stability and lifetime can be increased while maintaining the solubility. These compounds can be used in various organic devices such as organic light emitting diodes, photovoltaic cells or organic semiconductor devices.