45592-46-9 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
N-ethylcyclopentanamine serves as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure allows it to be a key component in the development of new drugs and agricultural products, contributing to advancements in these fields.
Used as a Corrosion Inhibitor:
In the industrial sector, N-ethylcyclopentanamine is utilized as a corrosion inhibitor. Its ability to protect metal surfaces from corrosion makes it a valuable asset in industries where metal components are exposed to corrosive environments, thereby extending the lifespan of equipment and reducing maintenance costs.
Used as a Solvent for Resins and Dyes:
N-ethylcyclopentanamine also functions as a solvent for resins and dyes. Its solubility properties enable it to dissolve a wide range of substances, making it useful in applications such as paint and coating formulations, as well as in the dyeing of textiles. This versatility in solubility contributes to its utility across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 45592-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,5,9 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 45592-46:
(7*4)+(6*5)+(5*5)+(4*9)+(3*2)+(2*4)+(1*6)=139
139 % 10 = 9
So 45592-46-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H15N/c1-2-8-7-5-3-4-6-7/h7-8H,2-6H2,1H3
45592-46-9Relevant academic research and scientific papers
ELECTROCHEMICAL REDUCTIVE AMINATION. I. AMINATION OF ALIPHATIC KETONES BY PRIMARY AMINES
Smirnov, Yu. D.,Tomilov, A. P.
, p. 42 - 48 (2007/10/02)
The reductive amination of aliphatic ketones in aqueous solutions of primary amines was realized by an electrochemical method.The best yields of the secondary amines were obtained at lead and cadmium cathodes in an aqueous electrolytic solution at pH 11-12.Elongation and branching in the carbon chain of the radicals both of the ketone and of the primary amine lead to a reduction in the yield of the secondary amine.The yield of the secondary amine is mainly determined by the rate of the chemical reaction leading to the formation of the azomethine compound, preceding the electrochemical reduction stage.
