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Benzene, 1,3-dinitroso-, also known as 1,3-dinitroso-benzene or DNB, is an organic compound with the chemical formula C6H4N2O4. It is a yellow crystalline solid that is soluble in water and has a melting point of 89-90°C. DNB is a derivative of benzene, where two nitroso groups (-NO) are attached to the 1 and 3 positions of the benzene ring. Benzene, 1,3-dinitroso- is primarily used as a chemical intermediate in the synthesis of various dyes, pharmaceuticals, and other organic compounds. Due to its reactivity and potential health hazards, DNB is handled with caution and is considered a hazardous substance.

7259-71-4

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7259-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7259-71-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7259-71:
(6*7)+(5*2)+(4*5)+(3*9)+(2*7)+(1*1)=114
114 % 10 = 4
So 7259-71-4 is a valid CAS Registry Number.

7259-71-4Upstream product

7259-71-4Downstream Products

7259-71-4Relevant academic research and scientific papers

Reduction of nitro aromatic compounds by zero-valent iron metal

Agrawal, Abinash,Tratnyek, Paul G.

, p. 153 - 160 (1996)

The properties of iron metal that make it useful in remediation of chlorinated solvents may also lead to reduction of other groundwater contaminants such as nitro aromatic compounds (NACs). Nitrobenzene is reduced by iron under anaerobic conditions to aniline with nitrosobenzene as an intermediate product. Coupling products such as azobenzene and azoxybenzene were not detected. First-order reduction rates are similar for nitrobenzene and nitrosobenzene, but aniline appearance occurs more slowly (typical pseudo-first-order rate constants 3.5 x 10-2, 3.4 x 10-2, and 8.8 x 10- 3 min-1, respectively, in the presence of 33 g/L acid-washed, 18-20 mesh Fluka iron turnings). The nitro reduction rate increased linearly with concentration of iron surface area, giving a specific reaction rate constant (3.9 ± 0.2 x 10-2 min-1 m-2 L). The minimal effects of solution pH or ring substitution on nitro reduction rates, and the linear correlation between nitrobenzene reduction rate constants and the square-root of mixing rate (rpm), suggest that the observed reaction rates were controlled by mass transfer of the NAC to the metal surface. The decrease in reduction rate for nitrobenzene with increased concentration of dissolved carbonate and with extended exposure of the metal to a particular carbonate buffer indicate that the precipitation of siderite on the metal inhibits nitro reduction.

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