65344-26-5

Basic information

• Product Name: 4-Iododibenzo-[b,d]furan
• Synonyms: 4-Iododibenzo-[b,d]furan;4-Iododibenzofuran;Dibenzofuran, 4-iodo-
• CAS NO: 65344-26-5
• Molecular Formula: C₁₂H₇IO
• Molecular Weight: 294.08785
• Mol File: 65344-26-5.mol

Chemical Properties

• Melting Point: 73°C(lit.)
• Boiling Point: 366.6±15.0 °C(Predicted)
• Appearance: /
• Density: 1.809±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• CAS DataBase Reference: 4-Iododibenzo-[b,d]furan(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Iododibenzo-[b,d]furan(65344-26-5)
• EPA Substance Registry System: 4-Iododibenzo-[b,d]furan(65344-26-5)

Safety Data

• Hazardous Substances Data: 65344-26-5(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Synthesis:
4-Iododibenzo-[b,d]furan is utilized as a precursor in the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the creation of new drugs, contributing to the development of novel therapeutic agents.
Used in Organic Compound Synthesis:
Beyond pharmaceuticals, 4-Iododibenzo-[b,d]furan is also employed in the synthesis of other organic compounds. Its versatility in chemical reactions makes it a valuable intermediate in organic chemistry for producing a range of different molecules.
Used in Research and Development:
In the realm of research and development, 4-Iododibenzo-[b,d]furan is studied for its potential applications in creating new materials and technologies. Its unique properties may contribute to advancements in various scientific fields.
Used in Environmental and Safety Studies:
Given its known toxicity and environmental impact, 4-Iododibenzo-[b,d]furan is also used in studies aimed at understanding and mitigating its hazards. This includes research into safe handling procedures, disposal methods, and potential environmental remediation strategies.

Upstream product

• 132-64-9 dibenzofuran 
• 67-66-3 chloroform 
• 7553-56-2 iodine 
• 100124-06-9 4-dibenzofurylboronic acid 

Downstream Products

• 743453-07-8 N-(dibenzofuran-4-yl)-N-phenyl-amine 
• 1252914-30-9 N,N'-bis(dibenzofuran-4-yl)-N,N'-diphenyl-pyrene-1,6-diamine 
• 1010068-85-5 (6-phenyldibenzo[b,d]furan-4-yl)boronic acid 
• 1435893-13-2 2-(6-phenyldibenzo[b,d]furan-4-yl)pyridine 
• 1435893-76-7 C₄₅H₃₀IrN₃O 
• 7320-53-8 4-methyl-dibenzofuran 
• 51412-72-7 dibenzo-[b,d]furan-4-carbonitrile 
• 1338919-70-2 12H-benzofuro[2,3-a]carbazole 

Relevant articles and documents

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

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The present invention relates to a heterocyclic compound represented by chemical formula A, and an organic light-emitting device containing the same. The ring A, R11-R14, W, X, Y, and Z are the same as defined in the present specification. According to the present invention, the heterocyclic compound exhibits long lifespan and low voltage driving properties when used as a material for phosphorescent hosts.COPYRIGHT KIPO 2017

DIBENZOFURAN AND DIBENZOTHIOPHENE DERIVATIVES AND ORGANIC LIGHT-EMITTING DEVICES CONTAINING THEM

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COMPOUND AND ORGANIC ELECTROLUMINESCENT ELEMENT

PROBLEM TO BE SOLVED: To provide a novel compound that is high in band gap and T1 energy, has excellent electrical stability/thermal stability, and can be used also for a hole transport layer of an organic EL element, and to provide an organic EL element that comprises a hole transport layer comprising the compound, and has a longer life and high luminous efficiency. SOLUTION: The present invention provides a compound represented by formula (1) [where X1 to X4 each independently represent H, or a specific dibenzofuran; at least one of X1 to X4 is a specific dibenzofuran; R1 to R6 each independently represent H, a substituted/unsubstituted alkyl group or halogen group; Y is a substituted/unsubstituted an aromatic cyclic group]. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT

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HOLE TRANSPORT MATERIAL

PROBLEM TO BE SOLVED: To provide a compound large in band gap, excellent in electrical stability and thermal stability and capable of being used for a hole transport material of an organic EL element, and an organic EL element having long life and high luminous efficacy and having a hole transport material containing the compound. SOLUTION: There is provided a compound represented by the formula (1). In the formula (1), R1 to R4 are each independently H, a substituted or unsubstituted alkyl group or a halogen group, R1 to R4 may exist each independently single or plurality, and may be same or different when exist plurality, X1 and X2 are each independently substituted or unsubstituted aromatic cyclic group, Z1 and Z2 are each O or S, and n is an integer of 1 to 8. COPYRIGHT: (C)2016,JPOandINPIT