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4'-Methyl-2,4-dinitroazobenzene, also known as DNB or dinitrobenzene, is an organic compound with the chemical formula C7H6N4O4. It is a yellow crystalline solid that is soluble in organic solvents but not in water. This chemical is primarily used as a chemical intermediate in the synthesis of dyes, pigments, other and organic compounds. It is also known for its mutagenic and carcinogenic properties, making it a potential health hazard. Due to its hazardous nature, it is important to handle 4'-methyl-2,4-dinitroazobenzene with proper safety measures and to be aware of its environmental and health risks.

6562-26-1

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6562-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6562-26-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,6 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6562-26:
(6*6)+(5*5)+(4*6)+(3*2)+(2*2)+(1*6)=101
101 % 10 = 1
So 6562-26-1 is a valid CAS Registry Number.

6562-26-1Downstream Products

6562-26-1Relevant academic research and scientific papers

A New and Regioselective Synthesis of Aromatic Diazene Derivatives

Neumann, Wilhelm P.,Wicenec, Christian

, p. 2297 - 2301 (2007/10/02)

A new method for the preparation of aromatic diazene derivatives 3a-l, 5, 7a, b, 9 under very mild conditions is described.The reaction of trialkylarylstannanes with nitro-substituted benzenediazonium tetrafluoroborates leads, by strict ipso substitution, to the corresponding diaryldiazenes in satisfactory to high yields.Due to the excellent leaving group quality of the stannyl group azo compounds may be prepared which are not accessible by normal electrophilic azo coupling.The products can be valuable precursors, obtained by reduction of the amines or other derivatizations, for consecutive aromatic compounds.Key Words: Aromatic substitution, electrophilic / Azo compounds, synthesis of / Diazonium compounds, aromatic, coupling reaction of, with trialkylarylstannanes / Trialkylarylstannanes, application of

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