Interesting facts
Interesting Facts about N-allylprop-2-en-1-amine
N-allylprop-2-en-1-amine is a fascinating organic compound that catches the interest of chemists due to its unique structure and potential applications. Here are some intriguing aspects of this compound:
- Structure and Reactivity: The presence of both allyl and amine functional groups in N-allylprop-2-en-1-amine contributes to its reactivity, making it a valuable intermediate in various organic synthesis reactions. The allylic moiety can participate in electrophilic addition reactions, while the amine can engage in nucleophilic substitution reactions.
- Polymerization Potential: This compound is a candidate for polymerization reactions, especially in the production of polymers with specific properties. Chemists often explore its use in creating hydrogels or other materials that could be tuned for biocompatibility.
- Applications in Medicine: Compounds similar to N-allylprop-2-en-1-amine are studied for their potential pharmaceutical applications, particularly in the development of drugs targeting various metabolic pathways. The amine group can enhance the biological activity of molecules by increasing their solubility and interactions with biological targets.
- Structure-Activity Relationship (SAR) Studies: The fascinating structural features of N-allylprop-2-en-1-amine allow for detailed SAR studies. Researchers can modify the compound's structure to explore how these changes impact its biological activity, paving the way for the design of more effective therapeutic agents.
- Environmental Impact: With a growing emphasis on sustainable chemistry, the synthesis of N-allylprop-2-en-1-amine may also lead to more eco-friendly processes in organic synthesis. This aligns with current trends seeking to minimize waste and utilize renewable resources.
The study of N-allylprop-2-en-1-amine is not just an exercise in understanding chemistry; it's a gateway into potential future innovations in materials science and pharmacology. As one researcher noted, "The allure of such compounds lies in the unknown; every bond can lead to a new discovery."
As the field of organic chemistry continues to evolve, compounds like N-allylprop-2-en-1-amine will undoubtedly play a significant role in paving the way for novel applications and discoveries.
Synonyms
Diallylamine
124-02-7
CCRIS 4776
HSDB 5471
N-2-PROPENYL-2-PROPEN-1-AMINE
UNII-N18EXB6V6P
EINECS 204-671-2
N18EXB6V6P
NSC 20948
UN2359
BRN 0773718
DTXSID1024918
AI3-15324
DIALLYLAMINE [MI]
NSC-20948
N,N-Di(2-propenyl)amine
(CH2=CHCH2)2NH
DTXCID704918
4-04-00-01060 (Beilstein Handbook Reference)
UN 2359
N-2-PROPENYL-2-PROPEN-1-AMINE [HSDB]
Di2propenylamine
Amine, diallyl
N2Propenyl2propen1amine
RefChem:132600
2Propen1amine, N2propenyl
204-671-2
DYUWTXWIYMHBQS-UHFFFAOYSA-N
2-Propen-1-amine, N-2-propenyl-
Di-2-propenylamine
2-Propen-1-amine, N-2-propen-1-yl-
bis(prop-2-en-1-yl)amine
N-prop-2-enylprop-2-en-1-amine
N-allylprop-2-en-1-amine
MFCD00008642
diprop-2-enylamine
Amine, diallyl-
CAS-124-02-7
diallyl amine
diallyl-amine
bis(allyl)amine
di-allyl amine
N,N-Diallylamine
N,N-diallyl amine
Diallylamine, 99%
N,N-Diallylamine #
prop-2-ene, 1-allylamino-
SCHEMBL22104
SCHEMBL22105
SCHEMBL45172
WLN: 1U2M2U1
CHEMBL3186706
AAA12402
BCP30054
NSC20948
STR01759
Tox21_201555
Tox21_303139
SBB060901
AKOS000119778
NCGC00249067-01
NCGC00257162-01
NCGC00259104-01
DB-041761
D0069
Diallylamine [UN2359] [Flammable liquid]
NS00019771
ST45255400
EN300-19612
F097633
Q1208441
F2190-0524
Z104474454
2-Propen-1-amine, N-2-propenyl- pound>>Di-2-propenylamine pound>>bis(prop-2-en-1-yl)amine
Solubility of N-allylprop-2-en-1-amine
N-allylprop-2-en-1-amine, with its unique structure, exhibits intriguing solubility characteristics that are influenced by its functional groups and overall polarity. Typically, this compound is classified as:
This solubility behavior illustrates an important property:
Several factors can further affect its solubility:
In summary, N-allylprop-2-en-1-amine displays a versatile solubility profile, making it applicable in various chemical processes where solubility is a crucial factor.