124782-15-6

Basic information

• Product Name: HEXABENZILISOVYURTSITAN
• Synonyms: HEXABENZILISOVYURTSITAN
• CAS NO: 124782-15-6
• Molecular Formula: C₄₈H₄₈N₆
• Molecular Weight: 708.93
• Mol File: 124782-15-6.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: HEXABENZILISOVYURTSITAN(CAS DataBase Reference)
• NIST Chemistry Reference: HEXABENZILISOVYURTSITAN(124782-15-6)
• EPA Substance Registry System: HEXABENZILISOVYURTSITAN(124782-15-6)

Safety Data

• Hazardous Substances Data: 124782-15-6(Hazardous Substances Data)

Upstream product

• 4845-50-5 2,3-dihydroxy-1,4-dioxane 
• 100-46-9 benzylamine 
• 131543-46-9 Glyoxal 
• 46924-37-2 N,N'-Dibenzyl-1,2-ethanediimine 
• 124782-22-5 1,2-Bis(benzylamino)-1,2-ethanediol 
• 28227-42-1 1,4-di-tert-butyl-1,4-diazabutadiene 

Downstream Products

• 4238-71-5 1-benzylimidazole 
• 42164-42-1 1,3-dibenzyl-1,3-diazolidine 
• 1034-11-3 N,N'-dibenzylpiperazine 
• 103-67-3 benzyl-methyl-amine 
• 100-46-9 benzylamine 
• 166046-53-3 2,6,8,12-tetraacetyl-4,10-dibenzyl-2,4,5,8,10,12-hexaazatetracyclo[5.5.0.0^3,11.0^5,9]dodecane 
• 21037-12-7 1,3-dibenzylimidazolidine-2,4,5-trione 

Relevant articles and documents

Reductive debenzylation of hexabenzylhexaazaisowurtzitane - The key step of the synthesis of polycyclic nitramine hexanitrohexaazaisowurtzitane

Main features of the reductive debenzylation of 2,4,6,8,10,12-hexabenzyl-2, 4,6,8,10,12-hexaazaisowurtzitane were studied. This process is the key step of the synthesis of 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazatetracyclo[5.5.0. 03,11.0s

Novel approach for the synthesis of hexaazaisowurtzitane derivatives

A novel synthetic route to hexaazaisowurtzitane derivatives via transimination of N,N0-di-t-butyl- 1,2-ethanediimine with benzylamine, allylamine, and furfurylamine is reported.

Green Synthesis Using Tragacanth Gum and Characterization of Ni–Cu–Zn Ferrite Nanoparticles as a Magnetically Separable Catalyst for the Synthesis of Hexabenzylhexaazaisowurtzitane Under Ultrasonic Irradiation

In this work, we report the synthesis, characterization, and catalytic evaluation of Ni–Cu–Zn ferrite using tragacanth gum as a biotemplate and metal nitrates as the metal source by the sol-gel method without using any organic chemicals. The sample is cha

Cage amines as the stopper inhibitors of cholinesterases

Cage amines 1-4 are potent peripheral anionic site-bound reversible inhibitors of both acetylcholinesterase and butyrylcholinesterase. Cage amines 1-3 are selective butyrylcholinesterase inhibitor versus acetylcholinesterase. For both enzymes, the -log K

Catalitic synthesis of caged polynitramine compounds

An improved method of preparing 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane (2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazatetracyclo[5.5.0.05,9.03,11]dodecane) (HNIW) is disclosed. The compound is useful as a high ener

Synthesis of CL-20 by clean nitrating agent dinitrogen pentoxide

CL-20 is a high energy material. It is usually prepared via nitration with concentrated nitric and sulfuric acid, but this technique pollutes the environment. In this article, CL-20 was synthesized with 2,6,8,12- tetraacetylhexaazatetracyclo[5,5,0,03

Studies of the Synthesis, Protonation and Decomposition of 2,4,6,8,10,12-Hexabenzyl-2,4,6,8,10,12-hexaazatetracyclo5,9.03,11>dodecane (HBIW)

Reaction of glyoxal with benzylamine or with substituted benzylamines leads to the cage structure 3.The X-ray crystal structure of 3c formed from 4-chlorobenzylamine is reported. 1H and 13C NMR spectra of 3a-j have been measured.Changes in spectrs in the

Polyazapolycyclics by Condensation of Aldehydes with Amines. 2. Formation of 2,4,6,8,10,12-Hexabenzyl-2,4,6,8,10,12-hexaazatetracyclo5,9.03,11>dodecanes from Glyoxal and Benzylamines

The condensation of glyoxal with benzylamine leads to 2,4,6,8,10,12-hexabenzyl-2,4,6,8,10,12-hexaazatetracyclo5,9.03,11>dodecane (2a) in solvents such as acetonitrile or methanol with formic acid catalyst.Six phenyl-substitut