132034-89-0

Basic information

• Product Name: 4-Iododibenzothiophene
• Synonyms: 4-Iododibenzothiophene;4-Iododibenzo[b,d]thiophene
• CAS NO: 132034-89-0
• Molecular Formula: C₁₂H₇IS
• Molecular Weight: 310.15345
• Mol File: 132034-89-0.mol
• Article Data: 13

Chemical Properties

• Melting Point: 100.0 to 104.0 °C
• Boiling Point: 408.2±18.0 °C(Predicted)
• Appearance: /
• Density: 1.832±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• CAS DataBase Reference: 4-Iododibenzothiophene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Iododibenzothiophene(132034-89-0)
• EPA Substance Registry System: 4-Iododibenzothiophene(132034-89-0)

Safety Data

• Hazardous Substances Data: 132034-89-0(Hazardous Substances Data)

Usage

Chemical Properties

off-white powder

InChI:InChI=1S/C12H7IS/c13-10-6-3-5-9-8-4-1-2-7-11(8)14-12(9)10/h1-7H

Upstream product

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Downstream Products

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• 1203896-18-7 4-(bis(dibenzo[b,d]thiophen-4-yl)amino)phenol 
• 1345970-20-8 3-bromo-9-(dibenzo[b,d]thiophen-4-yl)-9H-carbazole 
• 1345143-35-2 9-(dibenzo thiophen-4-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole 
• 1252914-52-5 N-(dibenzothiophene-4-yl)-N-phenyl-amine 
• 222-21-9 12H-benzo[4,5]thieno[2,3-a]carbazole 
• 98251-31-1 4-phenyldibenzo[b,d]thiophene 
• 1345143-20-5 9-(dibenzo[b,d]thiophen-4-yl)-9?-phenyl-9H,9'H-3,3?-bicarbazole 
• 1397691-64-3 C₆₀H₃₇N₃S 
• 72433-66-0 dibenzo[b,d]thiophene-4-amine 

Relevant articles and documents

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COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

The present invention provides a compound of chemical formula 1 and an organic light emitting device comprising the same. The compound according to the present invention has excellent electrochemical and thermal stability, thereby having excellent lifespan characteristics.COPYRIGHT KIPO 2019

Synthesis of N -Aryl and N -Heteroaryl γ-, δ-, and ?-Lactams Using Deprotometalation-Iodination and N -Arylation, and Properties Thereof

Xanthone, thioxanthone, fluorenone, benzophenone, 2-benzoylpyridine, dibenzofuran, and dibenzothiophene were deprotonated using a base prepared in situ from MCl 2 ·TMEDA (M = Zn or Cd; TMEDA = N, N, N ′, N ′-tetramethylethylenediamine) and lithium 2,2,6,6-tetramethylpiperidide in a 1:3 ratio, as demonstrated by subsequent iodolysis. The different aryl halides were involved as partners in the N -arylation of pyrrolidin-2-one. In the presence of copper(I) iodide and tripotassium phosphate, and using dimethyl sulfoxide as solvent, the reactions could be performed in yields ranging from 40 to 70%. Most of the products were tested for their antimicrobial, antifungal, antioxidant, and cytotoxic (MCF-7) activity.