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CS-W001157 4
Total: USD 88.00

Cinnamyl Alcohol

  • CAS No. 104-54-1

  • Cat. No. CS-0008356
  • Purity≥95%
  • MDL No.MFCD00002921

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

Cinnamyl Alcohol|CS-0008356

Structure of 104-54-1

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General Information

  • CAS No. 104-54-1
  • Cat. No. CS-0008356
  • Purity ≥95%
  • MDL No. MFCD00002921
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₁₀O
  • Molecular Weight 134.18
  • Synonym(s) None
  • SMILES OC/C=C/C1=CC=CC=C1

Description

Cinnamyl alcohol is an organic building block used as a chain transfer agent in polymerization. Cinnamyl alcohol causes Friedel Crafts alkylation of bulky aromatic compound 2,4-di-tert-butylphenol using mesoporous aluminosilicate as catalyst. It undergoes partial oxidation in air to form cinnamaldehyde over a series of Bi-Pt/alumina catalysts. It is also used in perfumery and in deodorant compositions.Cinnamyl alcohol was used to study the alkylation of 2,4-di-tert-butylphenol by cinnamyl alcohol using aluminum-containing mesoporous ethane-silica catalyst. It was used to study gold nanoparticles supported on titanium dioxide catalysed oxidative coupling of alcohols and amines to form the corresponding imines.

Synthesis

  • Route1
    • null|null
      99441-44-8
    • ~99%
    • In-stock
      Cinnamyl Alcohol|CS-0008356
      104-54-1

    References

    • Morizawa, Yoshitomi; Mori, Ichiro; Hiyama, Tamejiro; Nozaki, Hitosi Synthesis, 1981 , # 11 p. 899 - 901
  • Route2

    References

    • Chemical Communications, , # 2 p. 241 - 243
  • Route3

    References

    • Morrill, Christie; Grubbs, Robert H. Journal of the American Chemical Society, 2005 , vol. 127, # 9 p. 2842 - 2843

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS02,GHS06,GHS08
Signal Word : Danger
UN#: 3077
Class : 9
Packing Group : Ⅲ
Hazard Statements : H302-H317-H411
Precautionary Statements : P261-P264-P270-P272-P273-P280-P302+P352-P330-P362+P364-P391-P501

Quality Control

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Computational Chemistry Data

  • TPSA   20.23
  • LogP   1.6921
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   2

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