125251-91-4

Basic information

• Product Name: 1,3,6,8-Tetraazatricyclo[4.3.1.13,8]undecane(9CI)
• Synonyms: 1,3,6,8-Tetraazatricyclo[4.3.1.13,8]undecane(9CI)
• CAS NO: 125251-91-4
• Molecular Formula: C7H14N4
• Molecular Weight: 154.21286
• Product Categories: TRIAZINE
• Mol File: 125251-91-4.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3,6,8-Tetraazatricyclo[4.3.1.13,8]undecane(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,6,8-Tetraazatricyclo[4.3.1.13,8]undecane(9CI)(125251-91-4)
• EPA Substance Registry System: 1,3,6,8-Tetraazatricyclo[4.3.1.13,8]undecane(9CI)(125251-91-4)

Safety Data

• Hazardous Substances Data: 125251-91-4(Hazardous Substances Data)

Usage

General Description

1,3,6,8-Tetraazatricyclo[4.3.1.13,8]undecane(9CI), also known as TATU, is a chemical compound with a unique tricyclic structure. It is a heterocyclic compound containing four nitrogen atoms and is known for its potential use as a ligand in coordination chemistry and as a building block for the synthesis of complex organic molecules. TATU has been studied for its ability to form stable complexes with transition metal ions and has shown promising applications in catalysis and material science. The compound is also of interest in pharmaceutical research for its potential therapeutic properties. Due to its distinctive structure and versatile reactivity, 1,3,6,8-Tetraazatricyclo[4.3.1.13,8]undecane(9CI) has attracted attention from scientists in various fields for its potential use in a wide range of applications.

Upstream product

• 50-00-0 formaldehyd 
• 107-15-3 ethylenediamine 
• 51-46-7 1,3,6,8-tetraazatricyclo[4.4.1.1^3,8]dodecane 

Relevant articles and documents

Preparation of cage amine 1,3,6,8-tetraazatricyclo[4.3.1.1 3,8]undecane

Reaction between cage amine 1,3,6,8-tetraazatricyclo[4.4.1.1 3,8]dodecane (TATD) and ammonium fluoride affords 1,3,6,8-tetraazatricyclo[4.3.1.13,8]undecane, the missing link between 1,3,5,7-tetraazatricyclo[3.3.1.13,7]deca

An NMR study of sequential intermediates and collateral products in the conversion of 1,3,6,8-tetraazatricyclo[4.4.1.13,8]dodecane (TATD) to 1,3,6,8-tetraazatricyclo[4.3.1.13,8]undecane (TATU)

In situ 1H nuclear magnetic resonance spectroscopy was used to investigate the processes that occur during the synthesis of 1,3,6,8-tetraazatricyclo[4.3.1.13,8]undecane (TATU). NMR analysis showed a reaction mixture containing more than one compound. The production of these intermediates and collateral products was rationally supported by a careful 1H NMR monitoring study. We characterized 1,3,5-triazabicyclo[3.2.1]octane (TABO, 4) and 3-(2-aminoethyl)-1,3,5-triazabicyclo[3.2.1]octane (AETABO, 7) by 1H and 13C NMR in D2O solution inside the NMR sample tube, as an intermediate and collateral product of the reaction, respectively. Further, a reaction of 1,3,6,8-tetraazatricyclo[4.4.1.13,8]dodecane (TATD) with 15N-labeled ammonium chloride was carried out. The 15N NMR and GC-MS experiments indicated that 15N was incorporated into TATU, TABO, and urotropine.