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CS-W001157 4
Total: USD 88.00

Triphenylborane

  • CAS No. 960-71-4

  • Cat. No. CS-0462774
  • Purity≥95%
  • MDL No.MFCD00003007

*For research and further manufacturing use only, not for direct human use.

Triphenylborane|CS-0462774

Structure of 960-71-4

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General Information

  • CAS No. 960-71-4
  • Cat. No. CS-0462774
  • Purity ≥95%
  • MDL No. MFCD00003007
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₈H₁₅B
  • Molecular Weight 242.12
  • Synonym(s) Triphenylboronsodiumhydroxideadductaqueoussolutionsligh
  • SMILES C1=CC=C(C=C1)B(C2=CC=CC=C2)C3=CC=CC=C3

Description

t-Boc-Aminooxy-PEG3-S-Ac is a hydrophilic PEG moiety containing a t-Boc aminooxy group and a sulfur acetyl group. The t-Boc group is acid labile. The sulfur acetyl group can be deprotected to generate a thiol compound. The PEG linker increases the water solubility of the compound in aqueous environments.

Synthesis

  • Route1
    • Copper(1+),tris(triphenylphosphine)-,tetraphenylborate(1-)(1:1)|CS-0634347
      34013-06-4
    • ~0%
    • Bis(triphenylphosphine)(phenyldihiocarboxylato)copper(I)|CS-1179434
      74468-53-4
    • In-stock
      Triphenylborane|CS-0462774
      960-71-4

    References

    • Bianchini, Claudio; Ghilardi, Carlo A.; Meli, Andrea; Orlandini, Annabella Inorganic Chemistry, 1983 , vol. 22, p. 2188 - 2191
  • Route2
    • null|null
      134882-83-0
    • ~%
    • null|null
      104453-08-9
    • In-stock
      Triphenylborane|CS-0462774
      960-71-4

    References

    • Journal of the American Chemical Society, , vol. 115, # 5 p. 1753 - 1759
  • Route3
    • null|null
      19287-45-7
    • ~%
    • In-stock
      Triphenylborane|CS-0462774
      960-71-4

    References

    • Gmelin Handbook: B: SVol.1, 4.8.3, page 219 - 224

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS02
Signal Word : Danger
UN#: 1325
Class : 4.1
Packing Group : Ⅱ
Hazard Statements : H228
Precautionary Statements : P210-P240-P241-P280-P370+P378

Quality Control

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Computational Chemistry Data

  • TPSA   0
  • LogP   2.2028
  • H_Acceptors   0
  • H_Donors   0
  • Rotatable_Bonds   3

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