86532-14-1

Basic information

• Product Name: 4,4'-bidibenzo[b,d]furan
• Synonyms: 4,4'-bidibenzo[b,d]furan
• CAS NO: 86532-14-1
• Molecular Weight: 334.374
• Mol File: 86532-14-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4,4'-bidibenzo[b,d]furan(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4'-bidibenzo[b,d]furan(86532-14-1)
• EPA Substance Registry System: 4,4'-bidibenzo[b,d]furan(86532-14-1)

Safety Data

• Hazardous Substances Data: 86532-14-1(Hazardous Substances Data)

Upstream product

• 5332-24-1 3-bromoquinoline 
• 100124-06-9 4-dibenzofurylboronic acid 
• 109-04-6 2-bromo-pyridine 
• 132-64-9 dibenzofuran 

Downstream Products

• 88928-98-7 (19S,20S)-19,20-bis((phenylmethoxy)methyl)-27,28,29,30-tetramethoxy-18,21-dioxapentacyclo<21.3.1.1^2,6.1^7,11.1^12,16>triconta-1-(27),2,4,6(30),7,9,11(29),12,14,16(28),23,25-dodecaene 
• 88868-32-0 N,N''-(2,2',2'',2'''-tetramethoxy<1,1':3',1'':3'',1'''-quaterphenyl>-3,3'''-diyl)bis 
• 88868-22-8 2,2',2'',2'''-tetramethoxy-3,3'''-bis(tetrahydro-2-oxo-1(2H)-pyrimidinyl)-1,1':3',1'':3'',1'''-quaterphenyl 
• 88868-29-5 2,2',2'',2'''-tetraethoxy-<1,1':3',1'':3'',1'''-quaterphenyl>-3,3''' dicarboxylic acid 
• 88868-26-2 2,2',2'',2'''-tetramethoxy-<1,1':3',1'':3'',1'''-quaterphenyl>-3,3''' dicarboxylic acid 
• 88868-30-8 2,2',2'',2'''-tetraethoxy-<1,1':3',1'':3'',1'''-quaterphenyl>-3,3''' dimethanol 
• 88868-28-4 3,3'''-bis(bromomethyl)-2,2',2'',2'''-tetramethoxy-1,1':3',1'':3'',1'''-quaterphenyl 
• 88868-27-3 2,2',2'',2'''-tetramethoxy-<1,1':3',1'':3'',1'''-quaterphenyl>-3,3''' dimethanol 
• 88868-31-9 3,3'''-bis(bromomethyl)-2,2',2'',2'''-tetraethoxy-1,1':3',1'':3'',1'''-quaterphenyl 
• 88868-25-1 2,2',2'',2'''-tetrahydroxy-<1,1':3',1'':3'',1'''-quaterphenyl>-3,3''' dicarboxylic acid 

Relevant articles and documents

Ligand-free and heterogeneous palladium on carbon-catalyzed hetero-suzuki-miyaura cross-coupling

A ligand-free and heterogeneous palladium on carbon (Pd/C)-catalyzed hetero-SuzukiMiyaura coupling reaction has been developed. The protocol enables the construction of both heterocyclic-alicyclic and heterocyclic-heterocyclic biaryl derivatives in good to excellent yields. Furthermore, Pd/C could be reused. The time-course study clarified that palladium was leached into the reaction media as the reaction proceeded and then completely deposited on the carbon support.