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dibenzo[b,e][1,4]dioxine-2,8-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71400-36-7

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71400-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71400-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,0 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 71400-36:
(7*7)+(6*1)+(5*4)+(4*0)+(3*0)+(2*3)+(1*6)=87
87 % 10 = 7
So 71400-36-7 is a valid CAS Registry Number.

71400-36-7Downstream Products

71400-36-7Relevant academic research and scientific papers

A new porous organic polymer containing Tr?ger's base units: Evaluation of the catalytic activity in Knoevenagel condensation reaction

Coll, Deysma,Escalona, Néstor,Jessop, Ignacio A.,Martin-Trasanco, Rudy,Niebla, Vladimir,Ortiz, Pablo A.,Pérez, Edwin,Rodríguez-González, Fidel E.,Tagle, Luis H.,Terraza, Claudio A.,Tundidor-Camba, Alain,Velázquez-Tundidor, M. V.

, (2021)

The classic Tr?ger's base polymerization of a diamine and dimethoxymethane with trifluoroacetic acid as catalyst generated a Tr?ger's base-type polymer (TBP), which exhibited the absolute insolubility in a variety of organic solvents because of its highly aggregated model. A new porous organic polymer was obtained by a simple Tr?ger's base polymerization reaction between a diamine and formaldehyde in the form of acetal in the presence of trifluoroacetic acid as catalyst. Tr?ger's base-type polymer (TBP) resulted insoluble in a wide range of organic solvents due to its rigid and aromatic structure. TBP was characterized spectroscopically (FT-IR), thermally and morphologically. As result, a thermostable and amorphous polymer bearing pores ranging between 50 and 300 nm and macro-voids of up to 12 μm was obtained. Due to the insolubility of the TBP, it was tested as a metal-free heterogeneous catalyst in the Knoevenagel condensation reaction, showing a high efficiency. For this, the optimal catalyst load, reaction time and reuse of the catalyst were studied using benzaldehyde and malononitrile as substrates. Furthermore, aldehydes with variable chain sizes and ethyl cyanoacetate replacing malononitrile were tested as substrate with a high percent of conversion (97–99%).

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