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CS-W001157 4
Total: USD 88.00

Octylbenzene

  • CAS No. 2189-60-8

  • Cat. No. CS-0152266
  • Purity≥97%
  • MDL No.MFCD00009564

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

Octylbenzene|CS-0152266

Structure of 2189-60-8

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General Information

  • CAS No. 2189-60-8
  • Cat. No. CS-0152266
  • Purity ≥97%
  • MDL No. MFCD00009564
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₄H₂₂
  • Molecular Weight 190.32
  • Synonym(s) n-Octylbenzene, (1-Phenyloctane)
  • SMILES CCCCCCCCC1=CC=CC=C1

Description

Octylbenzene (1-Phenyloctane) forms charge-transfer complexes with fluoranil and 1,3,5-trinitrobenzene.1-Phenyloctane is used as a solvent to study the self-assembly of derivatives of tetrathiafulvalene (TTF) on graphite and their visualization by scanning tunnelling microscopy (STM). It is also used to study the effects of the substitution of these compounds on the interactions between them.

Synthesis

  • Route1
    • null|null
      111-85-3
    • In-stock
      Phenylboronic acid|CS-W001090
      98-80-6
    • ~84%
    • In-stock
      Octylbenzene|CS-0152266
      2189-60-8

    References

    • Sumitomo Chemical Co.,Ltd. Patent: EP1439157 A2, 2004 ; Location in patent: Page 9-11 ;
  • Route2
    • Octanophenone|CS-0064499
      1674-37-9
    • ~94%
    • In-stock
      Octylbenzene|CS-0152266
      2189-60-8

    References

    • Rahaim, Ronald J.; Maleczka, Robert E. Organic Letters, 2011 , vol. 13, # 4 p. 584 - 587
  • Route3

    References

    • Kirchhoff, Jan H.; Netherton, Matthew R.; Hills, Ivory D.; Fu, Gregory C. Journal of the American Chemical Society, 2002 , vol. 124, # 46 p. 13662 - 13663

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   0
  • LogP   4.5896
  • H_Acceptors   0
  • H_Donors   0
  • Rotatable_Bonds   7

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