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2-(2,4-dinitrophenyl)-1H-benzo[d]imidazole is a chemical compound with the molecular formula C13H7N5O5. It is a derivative of benzoimidazole, featuring a 2,4-dinitrophenyl group attached to the imidazole ring. 2-(2,4-dinitrophenyl)-1H-benzo[d]imidazole is known for its potential applications in various fields, such as pharmaceuticals and agrochemicals, due to its unique chemical structure and properties. The presence of the 2,4-dinitrophenyl group imparts significant reactivity and stability to the molecule, making it a subject of interest for researchers in the field of organic chemistry.

76463-20-2

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76463-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76463-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,6 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76463-20:
(7*7)+(6*6)+(5*4)+(4*6)+(3*3)+(2*2)+(1*0)=142
142 % 10 = 2
So 76463-20-2 is a valid CAS Registry Number.

76463-20-2Downstream Products

76463-20-2Relevant academic research and scientific papers

Hypervalent iodine promoted: Ortho diversification: 2-aryl benzimidazole, quinazoline and imidazopyridine as directing templates

Saha, Moumita,Das, Asish R.

supporting information, p. 941 - 955 (2020/02/15)

The mild and efficient palladium-catalyzed ortho C(sp2)-H diversification of (NH)-free 2-substituted benzimidazole, quinazoline, and imidazopyridine is reported using hypervalent iodine as the key reagent. Acetoxy, aryl, iodide and nitro functi

Oxidative kinetic self-sorting of a dynamic imine library

Osowska, Karolina,Miljanic, Ognjen S.

supporting information; experimental part, p. 724 - 727 (2011/04/12)

Dynamic libraries of [n × n] imine components spontaneously simplify during a slow oxidation reaction to produce only n discrete products. The selectivity of this self-sorting process is a consequence of different oxidation rates for various imines, while the dynamic nature of the library enables self-sorting to proceed with high efficiency.

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