1055197-69-7

Basic information

• Product Name: C₁₅H₂₀O
• Synonyms: C₁₅H₂₀O
• CAS NO: 1055197-69-7
• Molecular Weight: 216.323
• Mol File: 1055197-69-7.mol

Chemical Properties

• CAS DataBase Reference: C₁₅H₂₀O(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₅H₂₀O(1055197-69-7)
• EPA Substance Registry System: C₁₅H₂₀O(1055197-69-7)

Safety Data

• Hazardous Substances Data: 1055197-69-7(Hazardous Substances Data)

Upstream product

• 879-97-0 2,6-dimethyl-4-tert-butylphenol 
• 106-96-7 propargyl bromide 

Downstream Products

• 1055197-70-0 C₃₀H₂₈ClNO₂ 

Relevant articles and documents

Synthesis and evaluation of a novel fluorescent sensor based on?hexahomotrioxacalix[3]arene for Zn2+and Cd2+

A novel type of selective and sensitive fluorescent sensor having triazole rings as the binding sites on the lower rim of a hexahomotrioxacalix[3]arene scaffold in a cone conformation is reported. This sensor has desirable properties for practical applica

A Rare and Exclusive Endoperoxide Photoproduct Derived from a Thiacalix[4]arene Crown-Shaped Derivative Bearing a 9,10-Substituted Anthracene Moiety

A rare and exclusive endoperoxide photoproduct was quantitatively obtained from a thiacalix[4]arene crown-shaped derivative upon irradiation at λ=365 nm; the structure was unambiguously confirmed by 1H/13C NMR spectroscopy and X-ray crystallography. The prerequisites for the formation of the endoperoxide photoproduct have also been discussed. Furthermore, the photochemical reaction rate could be greatly enhanced in the presence of the thiacalix[4]arene platform because it served as a host to capture oxygen. It's a trap! A rare and exclusive endoperoxide photoproduct (E1) was quantitatively obtained from a thiacalix[4]arene crown-shaped derivative (T1) upon irradiation at λ=365 nm (see scheme). The photochemical reaction rate could be greatly enhanced in the presence of the thiacalix[4]arene platform because it served as a host to capture oxygen.

Highly selective fluorescent sensing of Cu2+ ion by an arylisoxazole modified calix[4]arene

A novel fluorescent chemosensor 1 with two anthraceneisoxazolymethyl groups at the lower rim of calix[4]arene has been synthesized, which revealed a dual emission (monomer and excimer) when excited at 375 nm. This chemosensor displayed a selective fluorescence quenching only with Cu2+ ion over all other metal ions examined. When Cu2+ ion was bound to 1, the fluorescence intensities of both monomer and excimer were quenched. Furthermore, the association constant for the 1:1 complex of 1·Cu2+ was determined to be (1.58 ± 0.03) × 104 M-1.