111-39-7 Usage
Description
N-(N-PROPYL)ETHYLENEDIAMINE, also known as N-Propylethylenediamine, is a clear colorless liquid with chemical properties that make it useful in various applications. It is an organic compound with the molecular formula C5H14N2 and is characterized by its amine functional groups.
Uses
Used in Chemical Synthesis:
N-(N-PROPYL)ETHYLENEDIAMINE is used as a chemical intermediate for the synthesis of various compounds, such as N-acetyl-N′-propylethylenediamine. This application takes advantage of its reactive amine groups, which can participate in a range of chemical reactions to produce desired products.
Used in Environmental Applications:
In the environmental sector, N-(N-PROPYL)ETHYLENEDIAMINE is used as a chelating agent for the quantitative removal of Cu(2+) ions from buffered solutions at pH 6. Its ability to form stable complexes with metal ions makes it an effective tool for heavy metal removal and wastewater treatment.
Used in Analytical Chemistry:
N-(N-PROPYL)ETHYLENEDIAMINE can be employed as a component in the development of analytical methods, such as high-performance liquid chromatography (HPLC) or capillary electrophoresis (CE), for the separation and detection of various compounds. Its unique chemical properties can enhance the selectivity and efficiency of these analytical techniques.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, N-(N-PROPYL)ETHYLENEDIAMINE may be utilized as a building block for the synthesis of drug candidates or as a reagent in the production of active pharmaceutical ingredients (APIs). Its versatility in chemical reactions allows for the creation of a wide range of molecular structures with potential therapeutic applications.
Used in Material Science:
N-(N-PROPYL)ETHYLENEDIAMINE can also find applications in the field of material science, where it may be used to modify the properties of polymers or to create new materials with specific characteristics. Its amine groups can interact with various substrates, leading to the development of materials with improved performance in areas such as adhesion, corrosion resistance, or thermal stability.
Check Digit Verification of cas no
The CAS Registry Mumber 111-39-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 111-39:
(5*1)+(4*1)+(3*1)+(2*3)+(1*9)=27
27 % 10 = 7
So 111-39-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H14N2/c1-2-4-7-5-3-6/h7H,2-6H2,1H3/p+2
111-39-7Relevant articles and documents
The synthesis of asymmetric ethylenediamine derivatives catalyzed by ion-exchange resins
Wang, Wenwen,Wei, Ruisong,Yin, Guohui,Tian, Jun,Duan, Yifan,Chen, Ligong,Li, Yang
, p. 4511 - 4522 (2015/06/30)
The ring-opening reaction of aziridine with alkylamines over a series of ion-exchange resins was investigated. Among these catalysts, D001-CC exhibited excellent catalytic performance. The catalysts were characterized by SEM and N2 adsorption-desorption. The results indicated that the selectivity of N,N-diethylethylenediamine mainly depended on the acidity and S BET of the resins. Strong Br?nsted acid sites played an important role on the conversion of aziridine, and the distribution of acid sites on catalyst had a significant effect on the selectivity of N,N-diethylethylenediamine. The reaction parameters, such as reaction time, molar ratio, reaction temperature, and catalyst loading, were also optimized and N,N-diethylethylenediamine was obtained in an excellent yield of 97 %. Furthermore, D001-CC was efficiently recycled five times by simple treatment with large amounts of deionized water and mineral acid. Finally, a series of asymmetric ethylenediamine derivatives were successfully synthesized with this method. Therefore, a simple and versatile process for the synthesis of asymmetric ethylenediamine derivatives has been established over ion-exchange resins.
N-alkylation of ethylenediamine with alcohols catalyzed by CuO-NiO/?3-Al2O3
Huang, Jia-Min,Xu, Lu-Feng,Qian, Chao,Chen, Xin-Zhi
, p. 304 - 307 (2015/03/03)
A simple method for N-alkylation of 1,2-diaminoethane with different alcohols in a fixed-bed reactor using cheap CuO-NiO/?3-Al2O3 as the catalyst has been developed. The present catalytic system was applicable in the N-alkylation of
Pyridylcarbonyl and thiocarbonyl derivatives useful as fungicides
-
, (2008/06/13)
The substituted heteroaryl compounds of this invention are good fungicides. In particular, they possess especially good activity against Bean Powdery Mildew, and other plant fungal diseases.
