16165-33-6 Usage
Uses
Used in Chemical Synthesis:
DI-N-UNDECYLAMINE is used as a reactant in the synthesis of symmetrical two-tailed dendritic tricarboxylato amphiphiles. These amphiphiles are important in the development of advanced materials, such as dendrimers, which have potential applications in drug delivery, nanotechnology, and other fields.
In the chemical industry, DI-N-UNDECYLAMINE serves as a key component in the production of various compounds, including surfactants, emulsifiers, and other specialty chemicals. Its unique structure allows it to form stable complexes with a wide range of molecules, making it a valuable asset in the synthesis of new materials.
Additionally, DI-N-UNDECYLAMINE can be used as a catalyst in certain chemical reactions, facilitating the formation of desired products with improved efficiency and selectivity. This application further highlights the versatility of DI-N-UNDECYLAMINE in the realm of chemical synthesis and process optimization.
Check Digit Verification of cas no
The CAS Registry Mumber 16165-33-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,6 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16165-33:
(7*1)+(6*6)+(5*1)+(4*6)+(3*5)+(2*3)+(1*3)=96
96 % 10 = 6
So 16165-33-6 is a valid CAS Registry Number.
InChI:InChI=1/C22H47N/c1-3-5-7-9-11-13-15-17-19-21-23-22-20-18-16-14-12-10-8-6-4-2/h23H,3-22H2,1-2H3
16165-33-6Relevant academic research and scientific papers
One-pot reductive amination of carboxylic acids: a sustainable method for primary amine synthesis
Coeck, Robin,De Vos, Dirk E.
supporting information, p. 5105 - 5114 (2020/08/25)
The reductive amination of carboxylic acids is a very green, efficient and sustainable method for the production of (bio-based) amines. However, with current technology, this reaction requires two to three reaction steps. Here, we report the first (heterogeneous) catalytic system for the one-pot reductive amination of carboxylic acids to amines, with solely H2 and NH3 as the reactants. This reaction can be performed with relatively cheap ruthenium-tungsten bimetallic catalysts in the green and benign solvent cyclopentyl methyl ether (CPME). Selectivities of up to 99% for the primary amine could be achieved at high conversions. Additionally, the catalyst is recyclable and tolerant for common impurities such as water and cations (e.g. sodium carboxylate).
