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3,7-bis(4-nitrophenyl)-1,5,3,7-dioxadiazocane is a complex organic compound characterized by its unique structure and properties. This molecule features a diazocane ring, which is a seven-membered ring containing two nitrogen atoms, and is adorned with two 4-nitrophenyl groups attached at the 3 and 7 positions. The 4-nitrophenyl groups contribute to the compound's chemical reactivity and stability, with the nitro group (-NO2) being a strong electron-withdrawing group that can influence the molecule's electronic properties. 3,7-bis(4-nitrophenyl)-1,5,3,7-dioxadiazocane is of interest in chemical research due to its potential applications in various fields, including the synthesis of pharmaceuticals and the development of new materials. Its specific properties, such as solubility, reactivity, and potential biological activity, make it a subject of study for chemists and material scientists.

857-94-3

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857-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 857-94-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,5 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 857-94:
(5*8)+(4*5)+(3*7)+(2*9)+(1*4)=103
103 % 10 = 3
So 857-94-3 is a valid CAS Registry Number.

857-94-3Downstream Products

857-94-3Relevant academic research and scientific papers

Synthesis and spectroscopic studies of diaza-8-crown-4-dinitrophenyl ethers

Galea, Claudia,Makuc, Damjan,Szaci?owski, Konrad,Plavec, Janez,Magri, David C.

, p. 13 - 22 (2020)

The macrocycles 3,7-bis(3-nitrophenyl)-1,5,3,7-dioxadiazocane 1 and 3,7-bis(4-nitrophenyl)-1,5,3,7-dioxadiazocane 2 were synthesised by a one-pot reaction with substituted nitroanilines and formaldehyde under acidic conditions. The same reaction with 2-ni

3,7-BIS-(4-TRIFLUOROMETHYLPHENYL)-1,5,3,7-DIOXADIAZOCINE: A NOVEL CYCLIC PRODUCT FROM A REACTION OF 4-TRIFLUOROMETHYLBENZENEDIAZONIUM CHLORIDE AND METHYLAMIN-FORMALDEHYDE

Kolar, George F.,Schendzielorz, Michael

, p. 1043 - 1044 (2007/10/02)

4-Substituted benzenediazonium chlorides react with methylamine-formaldehyde mixture at -5 to-10 deg C and controlled pH to afford the novel 3,7-bis-(4-X-aryl)-1,5,3,7-dioxadiazocines rather than the expected 1-(4-X-aryl)-3-hydroxymethyl-3-methyltriazenes or related dimeric products.

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