54008-40-1

Basic information

• Product Name: Germane, bis(pentafluorophenyl)-
• CAS NO: 54008-40-1
• Molecular Formula: C12H2F10Ge
• Molecular Weight: 408.722
• Mol File: 54008-40-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Germane, bis(pentafluorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Germane, bis(pentafluorophenyl)-(54008-40-1)
• EPA Substance Registry System: Germane, bis(pentafluorophenyl)-(54008-40-1)

Safety Data

• Hazardous Substances Data: 54008-40-1(Hazardous Substances Data)

Upstream product

• 10177-65-8 bis(pentafluorophenyl)germanium dibromide 
• 1188-14-3 Triethylgerman 
• 42371-50-6 tris(pentafuorophenyl)germane 
• 59871-31-7 1,1,1,3,3,3-Hexaethyl-2,2-bis(pentafluorphenyl)trigerman 
• 10360-39-1 tris(pentafluorophenyl)germanium bromide 
• 42437-33-2 hexakis(pentafluorophenyl)digermane 
• 69162-04-5 (C₆F₅)3GeBi(C₂H₅)2 
• 59871-30-6 1,1,1-Triethyl-2,2,2-tris-pentafluorophenyl-digermane 
• 69202-61-5 {(C₆F₅)3Ge}2BiC₂H₅ 
• 344-04-7 bromopentafluorobenzene 
• 16853-85-3 lithium aluminium tetrahydride 

Downstream Products

• 54008-42-3 bis-(pentafluoro phenyl) bromo germane 
• 59871-31-7 1,1,1,3,3,3-Hexaethyl-2,2-bis(pentafluorphenyl)trigerman 
• 102858-78-6 (C₅H₅)2VGe(H)(C₆F₅)2 
• 1333-74-0 hydrogen 
• 10177-70-5 hexakis-(pentafluoro phenyl) digermoxane 
• 1259-89-8 Chloro[tris(perfluorophenyl)]-germane 
• 54008-44-5 1,1,2,2-tetrakis-(pentafluoro phenyl) digermane 
• 10360-39-1 tris(pentafluorophenyl)germanium bromide 
• 53378-93-1 tris-(pentafluor phenyl) methoxy germane 
• 52057-32-6 tris-(pentafluoro phenyl) (trifluoro acetoxy) germane 
• 42437-33-2 hexakis(pentafluorophenyl)digermane 
• 10177-69-2 tris-(pentafluoro phenyl) germanol 
• 42371-50-6 tris(pentafuorophenyl)germane 
• 69162-04-5 (C₆F₅)3GeBi(C₂H₅)2 

Relevant articles and documents

donor-acceptor oligogermanes: Synthesis, structure, and electronic properties

A series of oligogermanes, (Me3Si)3GeGeCl 3, (C6F5)3GeGePh3, (C6F5)3GeGe(p-Tol)3, and (C 6F5)2Ge[Ge(p-Tol)3]2, containing substituents with different electronic properties at neighboring germanium atoms were synthesized. According to X-ray diffraction studies, UV/visible spectroscopy, and quantum chemical calculations, these donor-acceptor oligogermanes are characterized by energies of electronic transitions lower than those for other similar compounds.