Interesting facts
Interesting Facts about N',N'-diisopropylethane-1,2-diamine
N',N'-diisopropylethane-1,2-diamine, often referred to as DIPEA, is an intriguing compound in the field of organic chemistry. It's widely recognized for its role as a strong organic base used in various chemical reactions in laboratories. Here are some fascinating insights about this compound:
- Applications in Synthesis: DIPEA is commonly employed in the synthesis of pharmaceuticals and fine chemicals. Its ability to deprotonate acids makes it invaluable for facilitating reactions!
- Solvent Properties: This compound is also utilized as a solvent. Its unique chemical structure allows it to dissolve a wide range of compounds, making it essential in various chemical processes.
- Phase-Transfer Catalyst: Due to its properties, DIPEA can function as a phase-transfer catalyst, aiding in the migration of reactants from one phase to another during chemical reactions.
- Biological Importance: Beyond synthetic applications, DIPEA also plays a role in biological systems, being used to stabilize enzymes or as a reagent in biochemistry.
- Safety Protocols: When working with DIPEA, safety precautions are crucial. Proper handling and understanding of its reactivity profile help in minimizing risks associated with its usage.
- Structural Features: The presence of multiple isopropyl groups in its structure contributes to its steric bulk, significantly influencing the reaction pathways it participates in!
In summary, N',N'-diisopropylethane-1,2-diamine is not just a simple amine; its multifunctional roles in synthetic organic chemistry and biochemistry highlight the versatility and complexity of small organic molecules. As chemists delve deeper into its properties, new applications and innovative uses continue to emerge!
Synonyms
121-05-1
N,N-Diisopropylethylenediamine
2-Aminoethyldiisopropylamine
2-(Diisopropylamino)ethylamine
USAF AM-2
1,2-Ethanediamine, N,N-bis(1-methylethyl)-
N,N-Diisopropyl-1,2-ethanediamine
N1,N1-Diisopropylethane-1,2-diamine
N,N-Diisopropyl ethylenediamine
ETHYLENEDIAMINE, N,N-DIISOPROPYL-
N',N'-di(propan-2-yl)ethane-1,2-diamine
EINECS 204-447-4
NSC 166335
BRN 1734800
AI3-26667
2-DIISOPROPYLAMINOETHYLAMINE
1,2-Ethanediamine, N1,N1-bis(1-methylethyl)-
2-Aminoethyl diisopropylamine
4-04-00-01181 (Beilstein Handbook Reference)
(2-aminoethyl)bis(propan-2-yl)amine
NSC-166335
N,N-Bis(isopropyl)ethane-1,2-diamine
N,N-Bis(1-methylethyl)-1,2-ethanediamine
N1,N1-Bis(1-methylethyl)-1,2-ethanediamine
(2-aminoethyl)diisopropylamine
MFCD00015015
NSC166335
diisopropylaminoethylamine
EVU8JY5NTD
2-Aminoethyldiisopropylamin
Ethylenediamine,N-diisopropyl-
SCHEMBL151960
2-(Diisopropylamino)ethanamine
N, N-diisopropylethylenediamine
N,N-diisopropylethylene-diamine
N,N-Diisopropyl-ethylenediamine
2-(diisopropylamino)-ethylamine
2-diisopropylamino-1-ethylamine
1, N,N-bis(1-methylethyl)-
DTXSID2059518
N,N-diisopropyl ethylene diamine
CURJNMSGPBXOGK-UHFFFAOYSA-
n,n-diisopropyl-1,2-diaminoethane
N,N-diisopropylethane-1,2-diamine
N-(N,N-Diisopropylamino)ethylamine
BCP31428
STR07746
N,N-diisopropyl-ethane-1,2-diamine
AKOS000120778
N',N'-diisopropylethane-1,2-diamine
N1,N1-Diisopropyl-1,2-ethanediamine
[2-(Diisopropylamino)ethan-1-yl]amine
CS-W011005
n',n'-diisopropyl-ethane-1,2-diamine
SB75551
N,N-di(propan-2-yl)ethane-1,2-diamine
WLN: 1Y1 & M2MY1 & 1
DB-061850
D0006
NS00023947
EN300-20835
F11441
F2187-2163
N,N-Diisopropylethylenediamine;2-(Diisopropylamino)ethylamine
InChI=1/C8H20N2/c1-7(2)10(6-5-9)8(3)4/h7-8H,5-6,9H2,1-4H3
204-447-4
Solubility of N',N'-diisopropylethane-1,2-diamine
N',N'-diisopropylethane-1,2-diamine, with the formula C8H20N2, is known for its unique solubility characteristics. This compound is primarily soluble in a variety of organic solvents due to its structural attributes. Key points regarding its solubility include:
To summarize, N',N'-diisopropylethane-1,2-diamine is soluble in various organic media, with moderate water solubility. Its structural features play a significant role in determining its solubility in different environments, highlighting the intricate relationship between a compound's structure and its solubility behavior.