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2,6-dibenzyl-2,4,6,8-tetraazabicyclo[3,3,0]octan-3,7-dione is a complex organic compound with the molecular formula C20H24N4O2. It is a derivative of a bicyclic amine, specifically a tetraazabicyclo compound, which features a unique ring structure with four nitrogen atoms. The compound is characterized by the presence of two benzyl groups attached to the 2nd and 6th carbon atoms of the bicyclic structure, which contribute to its stability and potential applications. The 3,7-dione functional groups indicate the presence of two carbonyl groups, which can engage in various chemical reactions. 2,6-dibenzyl-2,4,6,8-tetraazabicyclo<3,3,0>octan-3,7-dione is of interest in the field of organic chemistry, potentially for its use in the synthesis of pharmaceuticals or other specialty chemicals, due to its unique structure and reactivity.

3721-08-2

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3721-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3721-08-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,2 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3721-08:
(6*3)+(5*7)+(4*2)+(3*1)+(2*0)+(1*8)=72
72 % 10 = 2
So 3721-08-2 is a valid CAS Registry Number.

3721-08-2Downstream Products

3721-08-2Relevant academic research and scientific papers

A search for synthetic routes to tetrabenzylglycoluril

Sinitsyna, Anastasia A.,Il’yasov, Sergey G.,Chikina, Maya V.,Eltsov, Ilia V.,Nefedov, Andrey A.

, p. 1019 - 1025 (2019/11/03)

In this study, a search for synthetic routes to never-before-seen tetrabenzylglycoluril was made and two synthetic strategies were examined: condensation of 1,3-dibenzylurea with glyoxal, and N-alkylation of glycoluril and its disubstituted derivative. The first synthetic approach furnished only a condensation product, 3,3′-bi(6,8-dibenzyl-2,4-dioxa-9,8-diazabicyclo[3.3.0]octan-7-one, bearing the dioxolane moiety, in 24% yield. The second method in which 2,6-dibenzylglycoluril was reacted with BnCl in acetonitrile in the presence of KOH for 3?h afforded the target product tetrabenzylglycoluril in over 60% yield.

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