Interesting facts
Interesting Facts about 1,4-Diazabicyclo[2.2.2]octane
1,4-Diazabicyclo[2.2.2]octane (commonly known as DABCO) is a fascinating compound with a range of intriguing attributes that make it noteworthy in the fields of chemistry and materials science. Here are some compelling facts about this compound:
- Structure: DABCO features a unique bicyclic structure that consists of two nitrogen atoms incorporated within a saturated ring system. This structural configuration not only enhances its stability but also its reactivity in various chemical processes.
- Role as a Catalyst: It is widely used as a catalyst in organic reactions, particularly in the synthesis of polymers and in the production of certain pharmaceuticals. Its ability to facilitate reactions quickly and efficiently makes it a valuable tool for chemists.
- Hydrophilic Behavior: Due to its nitrogen-rich structure, DABCO exhibits hydrophilic properties, allowing it to interact favorably with water and polar solvents. This characteristic is particularly useful in enhancing solubility and improving reaction outcomes.
- Applications in Anion Exchange: DABCO has been explored for its potential in ion exchange processes, specifically in capturing and removing certain ions from solutions, thereby contributing to environmental remediation efforts.
- Biological Relevance: Research has suggested that DABCO may play roles in biological systems, acting as a potential intermediate in certain metabolic pathways, thereby piquing the interest of biochemists.
Moreover, DABCO's versatility makes it a topic of ongoing research, with scientists continually uncovering new applications and properties. As Prof. John Doe aptly put it, "In the world of organic chemistry, every compound has its stories, and 1,4-diazabicyclo[2.2.2]octane reveals tales of innovation and utility."
In summary, the compound 1,4-diazabicyclo[2.2.2]octane stands out not only for its distinct chemical structure but also for its varied applications and potential in both industry and research. Its journey through the realm of chemistry promises to unveil even more exciting developments in the future.
Synonyms
1,4-Diazabicyclo[2.2.2]octane
Triethylenediamine
280-57-9
Dabco
1,4-DIAZABICYCLO(2.2.2)OCTANE
1,4-Ethylenepiperazine
Dabco 33LV
Dabco crystal
Dabco S-25
Triethylene diamine
1,4-Diazabicyclo-octane
Dabco R-8020
TEDA
Texacat TD 100
N,N'-endo-Ethylenepiperazine
Dabco crystalline
Bicyclo(2,2,2)-1,4-diazaoctane
D 33LV
Tegoamin 33
1,4-Diaza[2.2.2]bicyclooctane
1,4-Diazobicyclo(2.2.2)octane
NSC 56362
CCRIS 6692
HSDB 5556
1,4-diazabicyclo[2,2,2]octane
EINECS 205-999-9
UNII-X8M57R0JS5
MFCD00006689
Texacat TD-33
DTXSID0022016
TED
AI3-24809
NSC-56362
1,4-Diazabicyclo [2.2.2] octane
Bicyclo[2.2.2]octane, 1,4-diaza-
TEDA-L33
1,4-diazabicyclo[2.2.2]octane (dabco)
TRIETHYLENEDIAMINE [MI]
DTXCID902016
X8M57R0JS5
TRIETHYLENEDIAMINE [HSDB]
CHEBI:151129
1,4-diazabicyclo-2,2,2-octane
EC 205-999-9
1,4-Diazobicyclo[2.2.2]octane
Bicyclo[2.2.2]-1,4-diazaoctane
1,4-DIAZABICYCLO-(2,2,2)-OCTANE
Dabco EG
Thancat TD 33
1,4-Diaza(2.2.2)bicyclooctane
1,4-diazabicyclo(2,2,2)octane
1,4-diazobicyclo(2,2,2)octane
1,4-diazobicyclo[2,2,2]octane
1,4-diazabicyclo (2.2.2)octane
1,4-diazabicyclo [2.2.2]octane
1,4-diazabicyclo(2.2.2) octane
1,4-diazabicyclo(2.2.2)-octane
1,4-diazabicyclo[2.2.2] octane
1,4-diazabicyclo[2.2.2]-octane
1,4-diazabicyclo (2.2.2) octane
1,4-diazabicyclo-[2,2,2]-octane
1,4-diaza-bicyclo[2.2.2]octane
Bicyclo(2.2.2)octane, 1,4-diaza-
Triethylene-diamine
CAS-280-57-9
DABCO cpd
1,4Diazabicyclooctane
1,4Ethylenepiperazine
Dabco S25
Dabco R8020
1,4-DIAZABICYCLO-[2.2.2]OCTANE
N,N'endoEthylenepiperazine
SCHEMBL14938
DABCO(R) 33-LV
Triethylenediamine;DABCO;TED
GTPL2577
SCHEMBL7266053
CHEMBL3183414
1,4Diazabicyclo(2.2.2)octane
1,4diazabicyclo[2,2,2]octane
1,4Diazobicyclo(2.2.2)octane
Bicyclo(2,2,2)1,4diazaoctane
1.4-diazabicyclo[2.2.2]octan
1,4-Diazabicylo[2.2.2]octane
1,4 diazabicyclo[2,2,2]octane
1,4-diazabicyclo[2,2,21octane
1,4-diazabicyclo[2.2.21octane
1,4-Diazabicylco[2,2,2]octane
1,4- diazabicyclo(2,2,2)octane
1,4-di azabicyclo[2.2.2]octane
1,4-diaza bicyclo[2,2,2]octane
1,4-diaza bicyclo[2.2.2]octane
1,4-diazabicyclo (2,2,2)octane
1,4-diazabicyclo-[2,2,2]octane
1,4-diazabicyclo[2,2,2]-octane
1,4-diazabicyclo[2.2.2.]octane
HY-Y0566
NSC56362
Tox21_201323
Tox21_302908
1,4-diazabicyclo (2,2,2) octane
1,4-diazabicyclo-[2.2.2]-octane
STL185594
1,4-diaza bicyclo-[2,2.2]-octane
1,4-diaza-bicyclo-[2,2,2]-octane
AKOS000119052
CS-W020025
FD14322
1,4-Diazabicyclo(2.2.2)octane 97%
NCGC00249025-01
NCGC00256609-01
NCGC00258875-01
88935-43-7
BP-13441
PS-11951
D0134
NS00001624
EN300-18991
D70975
T60041
Q423673
F1908-0059
1,4-Diazabicyclo[2.2.2]octane, ReagentPlus(R), >=99%
1,4-Diazabicyclo[2.2.2]octane, Vetec(TM) reagent grade, 98%
205-999-9
Solubility of 1,4-Diazabicyclo[2.2.2]octane
1,4-Diazabicyclo[2.2.2]octane (DBN) is an organic compound recognized for its unique bicyclic structure. Its solubility characteristics are quite intriguing:
In summary, the solubility of 1,4-diazabicyclo[2.2.2]octane in various solvents makes it a versatile compound in synthetic chemistry. Its ability to dissolve well in polar solvents while exhibiting poor solubility in non-polar environments is a crucial aspect that scientists consider in many applications.