1084-26-0 Usage
Uses
Used in Organic Synthesis:
PTBPD is used as a building block in organic synthesis for the creation of novel organic materials. Its unique chemical structure and reactivity make it a valuable component in the synthesis of various organic compounds.
Used in Pharmaceutical Applications:
PTBPD is used as a potential active pharmaceutical ingredient due to its anti-inflammatory and antioxidant properties. It is being studied for its potential therapeutic effects in treating various conditions that involve inflammation and oxidative stress.
Used in Materials Science:
In the field of materials science, PTBPD is used as a component in the development of new materials with specific properties. Its chemical structure allows it to contribute to the formation of materials with tailored characteristics for various applications.
Used in Organic Electronics:
PTBPD is utilized in the development of organic electronic devices, such as organic light-emitting diodes (OLEDs) and organic solar cells, due to its electronic properties and compatibility with other organic materials.
Used in the Development of Dyes, Pigments, and Polymers:
Due to its unique chemical structure, PTBPD has potential applications in the creation of new dyes, pigments, and polymers. Its reactivity and color properties make it a promising candidate for use in the production of specialty chemicals for various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1084-26-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,8 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1084-26:
(6*1)+(5*0)+(4*8)+(3*4)+(2*2)+(1*6)=60
60 % 10 = 0
So 1084-26-0 is a valid CAS Registry Number.
1084-26-0Relevant academic research and scientific papers
Sterically controlled, palladium-catalyzed intermolecular amination of arenes
Shrestha, Ruja,Mukherjee, Paramita,Tan, Yichen,Litman, Zachary C.,Hartwig, John F.
supporting information, p. 8480 - 8483 (2013/07/19)
We report the Pd-catalyzed amination of arenes to form N-aryl phthalimides with regioselectivity controlled predominantly by steric effects. Mono-, di-, and trisubstituted arenes lacking a directing group undergo amination reactions with moderate to high yields and high regioselectivities from sequential addition of PhI(OAc)2 as an oxidant in the presence of Pd(OAc) 2 as catalyst. This sterically derived selectivity contrasts that for analogous arene acetoxylation.
Electrochemistry and Near-Infrared Spectra of Anion Radicals Containing Several Imide or Quinone Groups
Rak, Stanton F.,Jozefiak, Thomas H.,Miller, Larry L.
, p. 4794 - 4801 (2007/10/02)
A series of aromatic compounds possessing imide and quinone electron-acceptor groups were prepared using Diels-Alder reactions.These linear, aromatic compounds were studied using cyclic voltammetry and reduced electrochemically to produce solutions of the corresponding anion radicals.The anion radical near-infrared spectra were recorded and showed bands over the range 700-1700 nm (log ε 3.8-4.6).Most of the spectra are interpreted to arise from ?*-?* transitions.The spectra and Ε0 values are consistent with ground states in which the odd electron is delocalized over two electrophores.
