148892-95-9

Basic information

• Product Name: tris(2,3,5,6-tetrafluorophenyl)borane triethylphosphine oxide
• Synonyms: tris(2,3,5,6-tetrafluorophenyl)borane triethylphosphine oxide
• CAS NO: 148892-95-9
• Molecular Weight: 458.014
• Mol File: 148892-95-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: tris(2,3,5,6-tetrafluorophenyl)borane triethylphosphine oxide(CAS DataBase Reference)
• NIST Chemistry Reference: tris(2,3,5,6-tetrafluorophenyl)borane triethylphosphine oxide(148892-95-9)
• EPA Substance Registry System: tris(2,3,5,6-tetrafluorophenyl)borane triethylphosphine oxide(148892-95-9)

Safety Data

• Hazardous Substances Data: 148892-95-9(Hazardous Substances Data)

Upstream product

• 1094249-93-0 (Et₂O)B(p-C₆F₄H)3 
• 1094249-98-5 [(o-C₆H₄Me)3PH][HB(p-C₆F₄H)3] 
• 1559-88-2 1-bromo-2,3,5,6-tetrafluorobenzene 
• 1416345-33-9 C₂₀H₆BF₁₂N 
• 1416345-57-7 C₂₇H₁₃BF₁₂O₂ 
• 1109-15-5 tris(pentafluorophenyl)borate 
• 1239667-51-6 [(2,4,6-Me₃C₆H₂)3PH][HB(p-C₆F₄H)3] 

Downstream Products

• 1094249-94-1 (THF)B(p-C₆F₄H)3 
• 1094249-93-0 (Et₂O)B(p-C₆F₄H)3 
• 1094249-96-3 [t-Bu₃PH][HB(p-C₆F₄H)3] 
• 1094249-98-5 [(o-C₆H₄Me)3PH][HB(p-C₆F₄H)3] 
• 1094249-97-4 [Cy₃PH][HB(p-C₆F₄H)3] 
• 1239667-54-9 [(t-Bu)2(Cy)PH][HB(p-C₆F₄H)3] 
• 1239667-60-7 [(Ph₂CH)(i-Pr)2PH][HB(p-C₆F₄H)3] 
• 1239667-61-8 [(Ph₂CH)(Cy)2PH][HB(p-C₆F₄H)3] 
• 1239667-51-6 [(2,4,6-Me₃C₆H₂)3PH][HB(p-C₆F₄H)3] 
• 1239667-59-4 [(Ph₂CH)(t-Bu)2PH][HB(p-C₆F₄H)3] 
• 1239667-53-8 [(i-Pr)2(t-Bu)PH][HB(p-C₆F₄H)3] 
• 1239667-62-9 [(Ph₂CH)(C₅H₉)2PH][HB(p-C₆F₄H)3] 
• 1239667-50-5 [i-Pr₃PH][HB(p-C₆F₄H)3] 
• 1239667-52-7 [(t-Bu)2(i-Pr)PH][HB(p-C₆F₄H)3] 

Relevant articles and documents

Comparative Lewis acidity in fluoroarylboranes: B(o-HC6F 4)3, B(p-HC6F4)3, and B(C6F5)3

The Lewis acidic fluoroarylborane B(o-HC6F4) 3 (2) was prepared and its Lewis acid strength assessed in comparison to the known, related boranes B(C6F5)3 (1) and B(p-HC6F4/

Reversible, metal-free, heterolytic activation of H2 at room temperature

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Transition metal compound, catalyst for addition polymerization, and process for producing addition polymer

A transition metal compound (A) of the formula (1), a catalyst for addition polymerization obtained by bringing the transitionmetal compound to contact with (B) and/or (C) below, and a process for producing an addition polymer with the catalyst: wherein, M represents a titanium atom, zirconium atom or hafnium atom in the +3 formal oxide condition; A represents a multidentate mono-anionic ligand; R1 represents an alkyl group, aralkyl group, aryl group or substituted silyl group; E represents an oxygen atom or sulfur atom; each of two Xs independently represents a hydrogen atom, halogen atom, alkyl group, aralkyl group, aryl group, substituted silyl group, alkoxy group, aralkyloxy group, aryloxy group or di-substituted amino group, and two Xs may bond mutually to form a ring; D represents a neutral ligand coordinated on M; and n represents an integer of from 0 to 2.), (B)Organic aluminum compound and/or aluminoxane, (C)Specific boron compound.