134151-61-4

Basic information

• Product Name: 4,4'-[(1,2,3,3,4,4-HEXAFLUOROCYCLOBUTANE-1,2-DIYL)BIS(OXY)]DIBENZOIC ACID
• Synonyms: 4,4'-[(1,2,3,3,4,4-HEXAFLUOROCYCLOBUTANE-1,2-DIYL)BIS(OXY)]DIBENZOIC ACID
• CAS NO: 134151-61-4
• Molecular Formula: C₁₈H₁₀F₆O₆
• Molecular Weight: 436.26
• Mol File: 134151-61-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 513.2±50.0 °C(Predicted)
• Appearance: /
• Density: 1.67±0.1 g/cm3(Predicted)
• PKA: 4.15±0.10(Predicted)
• CAS DataBase Reference: 4,4'-[(1,2,3,3,4,4-HEXAFLUOROCYCLOBUTANE-1,2-DIYL)BIS(OXY)]DIBENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4'-[(1,2,3,3,4,4-HEXAFLUOROCYCLOBUTANE-1,2-DIYL)BIS(OXY)]DIBENZOIC ACID(134151-61-4)
• EPA Substance Registry System: 4,4'-[(1,2,3,3,4,4-HEXAFLUOROCYCLOBUTANE-1,2-DIYL)BIS(OXY)]DIBENZOIC ACID(134151-61-4)

Safety Data

• Hazardous Substances Data: 134151-61-4(Hazardous Substances Data)

Upstream product

• 134151-77-2 1-bromo-4-(trifluorovinyloxy)benzene 
• 106-41-2 4-bromo-phenol 
• 896431-10-0 1,2-bis(4-formylphenoxy)-hexafluorocyclobutane 
• 134151-66-9 4-(trifluorovinyloxy)benzoic acid 

Relevant articles and documents

METHOD OF MAKING PERFLUOROCYCLOBUTANE-CONTAINING MONOMER

The invention pertains to a multi-step process for making polyfunctional aromatic compounds comprising two phenyl rings bearing reactive groups susceptible of polycondensation reaction to provide polycondensed polymers, said method using economic raw materials, and possessing high selectivity and overall yield.

Synthesis and electronic factors in thermal cyclodimerization of functionalized aromatic trifluorovinyl ethers

A series of 19 p-substituted aromatic trifluorovinyl ether compounds were prepared from versatile intermediate P-Br-C6H4-O-CF= CF2 and underwent thermal radical mediated cyclodimerization to new difunctional compounds cont