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Cyanamide, also known as dicyandiamide, is an organic compound with the chemical formula NC(NH)2. It is a white crystalline solid that is used as a precursor in the production of melamine, a polymer used in plastics and resins. Cyanamide is also used in the synthesis of various chemicals, including cyanates and dithiocarbamates. 1,3,5-Triazine-2,4,6-triyltris is a cyclic compound with the chemical formula C3H3N6, which is composed of three triazine rings connected at their nitrogen atoms. Cyanamide,1,3,5-triazine-2,4,6-triyltris- is a key intermediate in the synthesis of various triazine-based compounds, such as herbicides and dyes. In summary, cyanamide and 1,3,5-triazine-2,4,6-triyltris are both important chemicals used in the production of various industrial materials and chemicals, with cyanamide being a precursor for melamine and 1,3,5-triazine-2,4,6-triyltris serving as an intermediate in the synthesis of triazine-based compounds.

4719-03-3

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4719-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4719-03-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,1 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4719-03:
(6*4)+(5*7)+(4*1)+(3*9)+(2*0)+(1*3)=93
93 % 10 = 3
So 4719-03-3 is a valid CAS Registry Number.

4719-03-3Downstream Products

4719-03-3Relevant academic research and scientific papers

Generation of melamine polymer condensates upon hypergolic ignition of dicyanamide ionic liquids

Chingin, Konstantin,Perry, Richard H.,Chambreau, Steven D.,Vaghjiani, Ghanshyam L.,Zare, Richard N.

experimental part, p. 8634 - 8637 (2011/11/07)

The reaction of dicyanamide ionic liquids with nitric acid results in hypergolic ignition and the formation of a stable precipitate. The precipitate consists of cyclic triazines, including melamine and its polymers, such as melam and melem (see scheme). This study introduces a novel approach to the synthesis of cyclic azines without resorting to high temperatures and pressures. Copyright

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