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1,4-Phenylenebis[(3-nitrophenyl)methanone], also known as 4,4'-(1,4-phenylene)bis(3-nitrobenzophenone), is an organic compound characterized by a central benzene ring with two nitrobenzophenone groups attached at the 1,4-positions. This molecule features a symmetrical structure, with each nitrobenzophenone group containing a benzene ring connected to a carbonyl group (C=O) and a nitro group (NO2). The presence of the nitro groups endows the compound with explosive properties, making it potentially hazardous. It is primarily used in the synthesis of high-energy materials and as a chemical intermediate in various industrial applications. Due to its reactivity and potential risks, handling and storage of 1,4-phenylenebis[(3-nitrophenyl)methanone] require strict safety measures and adherence to proper guidelines.

80213-65-6

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80213-65-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80213-65-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,1 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80213-65:
(7*8)+(6*0)+(5*2)+(4*1)+(3*3)+(2*6)+(1*5)=96
96 % 10 = 6
So 80213-65-6 is a valid CAS Registry Number.

80213-65-6Downstream Products

80213-65-6Relevant academic research and scientific papers

Efficient catalyst-free bi- and triaroylation of aromatic rings in a single step

Lo Fiego, Marcos J.,Badajoz, Mercedes A.,Silbestri, Gustavo F.,Lockhart, Maria T.,Chopa, Alicia B.

supporting information; scheme or table, p. 9184 - 9187 (2009/04/11)

(Chemical Equation Presented) The exceptional leaving group ability of the trimethylstannyl group in electrophilic aromatic substitutions makes possible the synthesis, in a single step, of bi- and triaroylarenes through the catalyst-free, regioselective reaction of bi- and tristannylarenes with different aroyl halides in o-dichlorobenzene as solvent. Specific di- and triketones are obtained in good to excellent yields (45-83%).

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