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CAS 6867-36-3

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(T-4)-[1,1′-Oxybis[ethane]]tris(pentafluorophenyl)boron

Description:
(T-4)-[1,1′-Oxybis[ethane]]tris(pentafluorophenyl)boron, with CAS number 6867-36-3, is a boron-containing compound characterized by its unique structure that includes a boron atom coordinated to three pentafluorophenyl groups and a bis(ethane) moiety linked through an ether bond. This compound exhibits significant thermal stability and is often utilized in various applications, including as a reagent in organic synthesis and as a potential catalyst in chemical reactions. The presence of multiple fluorinated phenyl groups contributes to its hydrophobic nature and enhances its electron-withdrawing properties, making it useful in electronic and material science applications. Additionally, the compound's unique electronic characteristics may facilitate its role in coordination chemistry and in the development of advanced materials. Its synthesis typically involves the reaction of boron trifluoride with appropriate organic precursors, and it is important to handle this compound with care due to the potential toxicity associated with fluorinated compounds.
Formula:C22H10BF15O
InChI:InChI=1S/C22H10BF15O/c1-3-39(4-2)23(5-8(24)14(30)20(36)15(31)9(5)25,6-10(26)16(32)21(37)17(33)11(6)27)7-12(28)18(34)22(38)19(35)13(7)29/h3-4H2,1-2H3
InChI key:InChIKey=VLTDIZAEUVUPMF-UHFFFAOYSA-N
SMILES:[B+3](O(CC)CC)([C-]=1C(F)=C(F)C(F)=C(F)C1F)([C-]=2C(F)=C(F)C(F)=C(F)C2F)[C-]=3C(F)=C(F)C(F)=C(F)C3F
Synonyms:
  • Boron, [1,1′-oxybis[ethane]]tris(pentafluorophenyl)-, (T-4)-
  • Borane, tris(pentafluorophenyl)-, compd. with ethyl ether (1:1)
  • (T-4)-[1,1′-Oxybis[ethane]]tris(pentafluorophenyl)boron
  • Tris(pentafluorophenyl)borane etherate
  • Borane, tris(pentafluorophenyl)-, compd. with diethyl ether
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