5410-97-9

Basic information

• Product Name: 3-Nitrodibenzofuran
• Synonyms: 3-NITRODIBENZOFURAN;3-Nitrodibenzo[b,d]furan;3-nitro-dibenzofura;Dibenzofuran, 3-nitro-;11-nitro-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(9),2,4,6,10,12-hexaene;NSC 10862
• CAS NO: 5410-97-9
• Molecular Formula: C₁₂H₇NO₃
• Molecular Weight: 213.19
• Product Categories: Fluorobenzene;Furans
• Mol File: 5410-97-9.mol
• Article Data: 30

Chemical Properties

• Melting Point: 181.5°C
• Boiling Point: 353.17°C (rough estimate)
• Flash Point: 183.4 °C
• Appearance: /
• Density: 1.2911 (rough estimate)
• Vapor Pressure: 1.26E-05mmHg at 25°C
• Refractive Index: 1.4500 (estimate)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 3-Nitrodibenzofuran(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Nitrodibenzofuran(5410-97-9)
• EPA Substance Registry System: 3-Nitrodibenzofuran(5410-97-9)

Safety Data

• Hazardous Substances Data: 5410-97-9(Hazardous Substances Data)

Usage

General Description

3-Nitrodibenzofuran is a chemical compound with the molecular formula C14H9NO3. It is a nitro-substituted dibenzofuran derivative, and it is mainly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. It is a yellow crystalline solid with a melting point of around 164-166°C. 3-Nitrodibenzofuran is known to have mutagenic and cytotoxic properties, and it has been studied for its potential use in anti-cancer treatments. However, its use is limited due to its potential toxicity and environmental concerns. Overall, 3-Nitrodibenzofuran is an important intermediate in organic synthesis, but its potential health and environmental risks warrant careful handling and disposal.

InChI:InChI=1/C12H7NO3/c14-13(15)8-5-6-10-9-3-1-2-4-11(9)16-12(10)7-8/h1-7H

Upstream product

• 132-64-9 dibenzofuran 
• 99586-25-1 3-nitro-dibenzofuran-2-carboxylic acid 
• 854395-60-1 7-nitro-dibenzofuran-4-carboxylic acid 
• 5422-92-4 1-amino-2-phenoxy-4-nitrobenzene 
• 104-82-5 4-Methylbenzyl chloride 
• 65103-30-2 4-nitrophenyl 2-(allyloxy)benzoate 
• 620-55-3 1-nitro-3-phenoxybenzene 
• 86607-75-2 C₁₂H₈BrNO₃ 
• 106961-16-4 2,4 DNP Phenol 
• 509-14-8 tetranitromethane 
• 56-23-5 tetrachloromethane 
• 7697-37-2 nitric acid 
• 64-19-7 acetic acid 
• 109-04-6 2-bromo-pyridine 

Downstream Products

• 5408-55-9 2,7-dinitrodibenzofuran 
• 26608-06-0 3-bromodibenzofuran 
• 133953-35-2 2,4-dibromodibenzofuran-3-amine 
• 29021-91-8 dibenzo[b,d]furan-3-carboxylic acid 
• 29021-90-7 dibenzo[b,d]furan-3-carbonitrile 
• 395087-89-5 2,2-dimethyl-5-phenyl-4H-benzo[d][1,3]dioxin-4-one 
• 1056113-50-8 2-(dibenzo[b,d]furan-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 51818-91-8 dibenzofuran-3-carboxaldehyde 
• 1342891-59-1 C₂₁H₁₈N₂O₄ 
• 1342891-58-0 C₂₂H₁₆N₂O₅ 
• 1080640-14-7 (S)-3-methyl-2-(8-(5-phenyl-1,2,4-oxadiazol-3-yl)dibenzo[b,d]furan-3-sulfonamido)butanoic acid 
• 1354827-67-0 C₂₅H₂₇N₃O₆S 

Relevant articles and documents

3-Nitrodibenzofuran and 3-Iododibenzofuran

The structures of 3-nitrodibenzofuran, C12H7NO3, and 3-iododibenzofuran, C12H7IO, have been determined.Both molecules are nearly planar and pack in herringbone patterns composed of symmetry related head-to-tail pairs with parallel ? systems.

NOVEL TRIAZINE COMPOUND, AND ORGANIC ELECTRONIC ELEMENT AND PLANT-GROWING LIGHTING THAT USE THE SAME

PROBLEM TO BE SOLVED: To provide a triazine compound which has a high triplet energy level and excellent heat resistance, and can be used as an organic electronic element material realizing an element with high efficiency, low voltage and a long life. SOLUTION: In the triazine compound, as represented by the general formula [1] in the figure, a triazine backbone moiety is linked to a dibenzofuran or dibenzothiophene backbone moiety via a biphenyl backbone moiety, where X is an oxygen atom or sulfur atom. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPO&INPIT

Microwave-Promoted Pd-Catalyzed Synthesis of Dibenzofurans from Ortho-Arylphenols

ortho-Aryl phenols, synthesized via protecting group free Suzuki–Miyaura coupling of ortho-halophenols and arene boronic acids, undergo a cyclization to dibenzofurans via oxidative C–H activation. The reaction proceeds under microwave irradiation in short reaction times using catalytic amounts of Pd(OAc)2 without additional ligands.