54470-37-0

Basic information

• Product Name: 1-Dibenzofurancarboxylic acid
• Synonyms: 1-Dibenzofurancarboxylic acid
• CAS NO: 54470-37-0
• Molecular Formula: C₁₃H₈O₃
• Molecular Weight: 212.2
• Mol File: 54470-37-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Dibenzofurancarboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Dibenzofurancarboxylic acid(54470-37-0)
• EPA Substance Registry System: 1-Dibenzofurancarboxylic acid(54470-37-0)

Safety Data

• Hazardous Substances Data: 54470-37-0(Hazardous Substances Data)

Upstream product

• 132-64-9 dibenzofuran 
• 124-38-9 carbon dioxide 
• 141104-58-7 dibenzo[b,d]furan-1-carbonitrile 
• 33483-06-6 1-hydroxydibenzofuran 
• 151-10-0 1,3-Dimethoxybenzene 
• 23112-96-1 (2,6-dimethoxyphenyl)boronic acid 
• 50548-38-4 1-bromo-N-(4-dibenzofuranyl)acetamide 
• 50548-37-3 N-(4-dibenzofuranyl)acetamide 
• 50548-39-5 1-bromodibenzo[b,d]furan-1-amine 
• 50548-43-1 4-aminodibenzofuran 
• 94538-00-8 1,3-Dichlorodibenzofuran 
• 7320-50-5 1-methyl-dibenzofuran 
• 50548-45-3 1-bromodibenzo[b,d]furan 

Relevant articles and documents

Novel antracene derivatives for organic light-emitting diode and organic light-emitting diode including the same

The present invention relates to an organic light emitting compound represented by chemical formula A, and an organic light emitting device comprising the same. Substituent R_1 to R_8, R_11 to R_19, L, n, and X are the same as defined in the specification. The organic light emitting compound represented by chemical formula A can be used as an organic light emitting device, and can be used to manufacture an excellent device having stable and highly efficient characteristics.COPYRIGHT KIPO 2016

Electrocarboxylation of chlorinated aromatic compounds

Chorinated benzenes (1, 4), biphenyls (6, 9), dibenzofurans (10, 15, 17, 18), 2-chlorodibenzo[1,4]dioxine (24) and 1-chloronaphthalene (26) as well as dibenzofuran (12) and naphthalene (27) themselves were transformed into carboxylic acids by galvanostatic electroreduction in the presence of carbon dioxide ("electrocarboxylation"). Dry DMF was used as solvent, zinc or stainless steel as cathode and magnesium as a sacrificial anode in an undivided cell. Hydrogenation of aromatic rings was not observed. However, reductive addition of two molecules of carbon dioxide to form dihydrodicarboxylic acids, e.g. 22 and 29, occurs in the dibenzofuran and naphthalene series.