96706-46-6

Basic information

• Product Name: DIBENZOFURAN-4-CARBOXALDEHYDE 97
• Synonyms: 4-dibenzofurancarboxaldehyde;dibenzo[b,d]furan-4-carbaldehyde(SALTDATA: FREE);Dibenzofuran-4-carboxaldehyde 97%;DIBENZOFURAN-4-CARBOXALDEHYDE 97;4-Dibezofurancarboxaldehyde;Dibenzo[b,d]furan-4-carboxaldehyde
• CAS NO: 96706-46-6
• Molecular Formula: C₁₃H₈O₂
• Molecular Weight: 196.2
• Product Categories: Benzofurans;Building Blocks;Heterocyclic Building Blocks
• Mol File: 96706-46-6.mol
• Article Data: 12

Chemical Properties

• Melting Point: 94-98 °F(lit.)
• Boiling Point: 360.5°Cat760mmHg
• Flash Point: 170.2°C
• Appearance: /
• Density: 1.289±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 2.21E-05mmHg at 25°C
• Refractive Index: 1.734
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: DIBENZOFURAN-4-CARBOXALDEHYDE 97(CAS DataBase Reference)
• NIST Chemistry Reference: DIBENZOFURAN-4-CARBOXALDEHYDE 97(96706-46-6)
• EPA Substance Registry System: DIBENZOFURAN-4-CARBOXALDEHYDE 97(96706-46-6)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 96706-46-6(Hazardous Substances Data)

Usage

General Description

Dibenzofuran-4-carboxaldehyde, also known as 4-Formyldibenzofuran, is a high-purity (97%) chemical compound that falls into the category of cyclic compounds and carbocycles. As with many chemicals, it is identified not only by its name but by a unique CAS (chemical abstracts service) registry number, in this case, 2743-38-6. It is typically used as a chemical intermediate in the synthesis of more complex chemical compounds. As with all chemicals, it needs to be handled and stored safely, wearing appropriate personal protective equipment (PPE) and used in a well-ventilated environment. Detailed safety and handling instructions can be found in its Material Safety Data Sheet (MSDS).

InChI:InChI=1/C13H8O2/c14-8-9-4-3-6-11-10-5-1-2-7-12(10)15-13(9)11/h1-8H

Upstream product

• 132-64-9 dibenzofuran 
• 68-12-2 N,N-dimethyl-formamide 
• 100124-06-9 4-dibenzofurylboronic acid 
• 298-12-4 Glyoxilic acid 
• 75-77-4 chloro-trimethyl-silane 
• 105478-94-2 4-bromomethyldibenzofuran 
• 93-61-8 N-methyl-N-phenylformamide 
• 16669-47-9 dibenzo[b,d]furan-4-yl lithium 
• 64102-19-8 dibenzo[b,d]furan-4-ylmethanol 
• 7320-53-8 4-methyl-dibenzofuran 
• 74-88-4 methyl iodide 

Downstream Products

• 1051445-42-1 4-dibenzofuranyl(phenyl)methanol 
• 1118667-98-3 (2Z)-3-dibenzo[b,d]furan-4-yl-2-phenylacrylic acid 
• 132-64-9 dibenzofuran 
• 99329-30-3 dibenzo[b,d]furan-4-yl(phenyl)methanone 

Relevant articles and documents

One-Pot Synthesis of Dissymmetrical 4,6-Disubstituted Dibenzofurans

The one-pot dissymmetrization of dibenzofuran has been achieved using directed ortho metallations.Effects of temperature, reaction time, stoichiometry of the lithiation reagent, and solvent were studied to obtain the best selectivity.

Method for producing an aromatic heterocyclic compound, organic semiconductor material and organic semiconductor device

PROBLEM TO BE SOLVED: To provide: an aromatic heterocyclic compound which has oxidation stability, high solubility, favorable film production properties and high charge transfer properties, and is suitable as an organic semiconductor material; and organic

An expedient osmium(vi)/K3Fe(CN)6-mediated selective oxidation of benzylic, allylic and propargylic alcohols

A chemoselective osmium(vi) catalyzed oxidation of benzylic, allylic and propargylic alcohols using K3Fe(CN)6as a secondary oxidant is described. This protocol is operationally simple and exhibits excellent chemoselectivity favouring the oxidation of benzylic alcohols over the aliphatic alcohols. A larger scale reaction was also found to be compatible. This journal is