3015-65-4 Usage
Uses
Used in Chemical Industry:
N,N-DIMETHYLTETRADECANAMIDE is used as a solvent in the production of polymers, resins, and coatings due to its suitability for high-temperature processes.
Used in Pesticide Formulation:
N,N-DIMETHYLTETRADECANAMIDE is utilized in the formulation of pesticides, contributing to the effectiveness and stability of these products.
Used in Pharmaceutical Formulation:
N,N-DIMETHYLTETRADECANAMIDE is also employed in the development of pharmaceuticals, where its properties can enhance the solubility and delivery of active ingredients.
It is crucial to handle N,N-DIMETHYLTETRADECANAMIDE with care, as improper management may lead to potential risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 3015-65-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,1 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3015-65:
(6*3)+(5*0)+(4*1)+(3*5)+(2*6)+(1*5)=54
54 % 10 = 4
So 3015-65-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H33NO/c1-4-5-6-7-8-9-10-11-12-13-14-15-16(18)17(2)3/h4-15H2,1-3H3
3015-65-4Relevant academic research and scientific papers
Aliphatic carboxylic acid amide preparation method
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Paragraph 0058; 0059; 0082; 0083, (2017/01/09)
The invention relates to a preparation method of aliphatic carboxylic acid amide. The method comprises the following step: carrying out a reaction on aliphatic carboxylic acid and monoalkylamine or dialkylamine with 1-4 carbon atoms in the presence of ceric oxide. By using the method, aliphatic carboxylic acid amide can be prepared with high yield, and a catalyst shows an excellent catalytic efficiency and reusing stability.
Regioselective hydrocarbamoylation of 1-alkenes
Miyazaki, Yosuke,Yamada, Yuuya,Nakao, Yoshiaki,Hiyama, Tamejiro
supporting information; experimental part, p. 298 - 300 (2012/05/20)
Nickel/Lewis acid cooperative catalysis derived from [Ni(cod)2], AlEt3, and N-heterocyclic carbene (NHC) effects highly regioselective hydrocarbamoylation of 1-alkenes. Variously substituted formamides and 1-alkenes can be employed to give a range of linear alkanamides regioselectively.
