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Hydroperoxide, 2-(4-methoxyphenyl)-4,5-diphenyl-4H-imidazol-4-yl, is a complex organic compound with the chemical formula C23H20N2O3. It is a derivative of imidazole, a heterocyclic aromatic organic compound, and features a hydroperoxide group attached to the imidazole ring. The molecule consists of a 4H-imidazol-4-yl core, with a 4-methoxyphenyl group at the 2-position and two phenyl groups at the 4 and 5 positions. Hydroperoxide, 2-(4-methoxyphenyl)-4,5-diphenyl-4H-imidazol-4-yl is known for its potential applications in various chemical reactions and processes, such as oxidation and synthesis of other organic compounds. Due to its unique structure and properties, it may also be of interest in the development of new materials and pharmaceuticals.

1914-97-2

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1914-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1914-97-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1914-97:
(6*1)+(5*9)+(4*1)+(3*4)+(2*9)+(1*7)=92
92 % 10 = 2
So 1914-97-2 is a valid CAS Registry Number.

1914-97-2Downstream Products

1914-97-2Relevant academic research and scientific papers

Evidence for the Formation of 1,2-Dioxetane as a High-Energy Intermediate and Possible Chemiexcitation Pathways in the Chemiluminescence of Lophine Peroxides

Boaro, Andreia,Reis, Roberta Albino,Silva, Carolina Santana,Melo, Diêgo Ulysses,Pinto, Alexander Garreta Gon?alves Costa,Bartoloni, Fernando Heering

, p. 6633 - 6647 (2021/05/29)

A kinetic study of the chemiluminescent (CL) reaction mechanism of lophine-derived hydroperoxides and silylperoxides induced by a base and fluoride, respectively, provided evidence for the formation of a 1,2-dioxetane as a high-energy intermediate (HEI) o

Location effect of an OH group on the chemiluminescence efficiency of 4-hydroperoxy-2-(o-, m-, or p-hydroxyphenyl)-4,5-diphenyl-4H-isoimidazoles

Tsunenaga, Mitsuru,Iga, Hiroshi,Kimura, Masaru

, p. 1877 - 1880 (2007/10/03)

In studying the location effect of an OH group on the chemiluminescence efficiency of 4-hydroperoxy-2-(o-, m-, or p-hydroxyphenyl)-4,5-diphenyl-4H- isoimidazoles 4, we found that the efficiency of 4a with o-OH was 0.28 times that of lophine peroxide on initiation with KOH/MeOH. When the trigger base was changed to TBAF/THF, efficiency was 530-fold in dry DMF. The efficiency of 4b with m-OH or 4c with p-OH showed no such dramatic change.

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