Interesting facts
Interesting Facts about N,N-Diallylprop-2-en-1-amine
N,N-Diallylprop-2-en-1-amine, with its intriguing structure and reactivity, is a fascinating compound often studied in the fields of organic and polymer chemistry. Below, we explore several interesting aspects of this compound:
- Reactivity: Due to the presence of both allyl and amine functional groups, N,N-diallylprop-2-en-1-amine exhibits unique reactivity patterns that make it valuable in various chemical reactions, particularly in polymerization processes.
- Applications: This compound is often used as a monomer in the synthesis of functional polymers, potentially resulting in materials with specialized properties such as enhanced thermal stability and flexibility.
- Catalyst Interaction: Researchers have noted the ability of N,N-diallylprop-2-en-1-amine to interact with various catalysts, enhancing the efficiency of certain reactions, making it an attractive option for industries focused on sustainable chemistry.
- Safety Precautions: While working with this compound, it's important to note that it may present some hazards. Proper handling and storage protocols are vital to ensuring safety in laboratory environments.
- Structural Insights: The unique arrangement of the allyl groups can lead to interesting stereochemical considerations, influencing its derivatization pathways and the ultimate properties of the resulting materials.
In conclusion, N,N-diallylprop-2-en-1-amine is more than just a simple compound; it opens doors to numerous applications and avenues of research in the world of chemistry. As the field evolves, the importance of understanding such compounds in depth cannot be overstated, making them a key area of interest for scientists and students alike.
Synonyms
TRIALLYLAMINE
102-70-5
Tris(2-propenyl)amine
2-Propen-1-amine, N,N-di-2-propenyl-
2-Propen-1-amine, N,N-di-2-propen-1-yl-
N,N-bis(prop-2-enyl)prop-2-en-1-amine
CCRIS 4876
N,N-Di-2-propenyl-2-propen-1-amine
N,N-diallylprop-2-en-1-amine
HSDB 2904
EINECS 203-048-2
UNII-B6N19XC04R
NSC 32635
UN2610
(CH2=CHCH2)3N
BRN 1740881
B6N19XC04R
DTXSID5026174
AI3-52705
NSC-32635
4-04-00-01061 (Beilstein Handbook Reference)
TRIALLYLAMINE [HSDB]
DTXCID506174
UN 2610
Triallyl Amine
tri-2-propenylamine
tris(prop-2-en-1-yl)amine
triallyl-amine
MFCD00026093
Tris(2propenyl)amine
Triallylamine, 99%
N,NDi2propenyl2propen1amine
SCHEMBL20656
prop-2-ene, 1-diallylamino-
2Propen1amine, N,Ndi2propenyl
CHEMBL3188834
CHEBI:192451
N,N-Diallyl-2-propen-1-amine #
NSC32635
Tox21_300670
2-Propen-1-amine,N-di-2-propenyl-
WLN: 1U2N2U1 & 2U1
AKOS015840489
NCGC00248135-01
NCGC00254578-01
CAS-102-70-5
LS-13670
N,N-bis(prop-2-enyl)-2-propen-1-amine
NS00021453
T0332
Triallylamine [UN2610] [Flammable liquid]
EN300-7644092
A800604
Q23779745
203-048-2
Solubility of N,N-diallylprop-2-en-1-amine
N,N-diallylprop-2-en-1-amine, a unique compound known for its dual allyl groups, exhibits interesting solubility characteristics:
In short, one can indeed say that "like dissolves like." The solubility of N,N-diallylprop-2-en-1-amine serves as a prime example of this principle, demonstrating the significance of functional groups in determining solubility behavior.