925-58-6 Usage
Uses
Used in Pharmaceutical Synthesis:
N-(2-aminoethyl)propanamide is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Production:
In the agrochemical industry, N-(2-aminoethyl)propanamide is utilized as a component in the synthesis of various agrochemicals, enhancing crop protection and yield.
Used as a Corrosion Inhibitor:
N-(2-aminoethyl)propanamide is used as a corrosion inhibitor, protecting metals from degradation and extending the lifespan of industrial equipment and structures.
Used as a Chelating Agent:
N-(2-aminoethyl)propanamide serves as a chelating agent, important for the removal of metal ions in various industrial processes, including water treatment and chemical analysis.
Used in Surfactant and Lubricant Production:
N-(2-aminoethyl)propanamide is used in the production of surfactants and lubricants, improving the performance and efficiency of these products in various applications.
Used in Textile Industry:
In the textile industry, N-(2-aminoethyl)propanamide is used to enhance the properties of fabrics, such as their softness, durability, and resistance to wear.
Used in Cosmetics and Personal Care Products:
N-(2-aminoethyl)propanamide is utilized in the formulation of cosmetics and personal care products, where it may contribute to improved texture, stability, and efficacy of the final products.
Check Digit Verification of cas no
The CAS Registry Mumber 925-58-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,2 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 925-58:
(5*9)+(4*2)+(3*5)+(2*5)+(1*8)=86
86 % 10 = 6
So 925-58-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H12N2O/c1-2-5(8)7-4-3-6/h2-4,6H2,1H3,(H,7,8)
925-58-6Relevant academic research and scientific papers
A two-step continuous-flow synthesis of n-(2-aminoethyl)acylamides through ring-opening/hydrogenation of oxazolines
Gutmann, Bernhard,Roduit, Jean-Paul,Roberge, Dominique,Kappe, C. Oliver
, p. 13146 - 13150 (2012/02/02)
Harnessing hydrazoic acid in flow! 2-Oxazolines can be ring-opened in a very efficient manner by treatment with in situ generated hydrazoic acid. Despite the toxic and explosive nature of hydrazoic acid, this process can be conducted safely in a continuou
SYNTHESIS OF ACYLATED (2'-HYDROXYETHYL)AMINO- AND (2'-AMINOETHYL)AMINO-1,3,5-TRIAZINES
Sapozhnikova, Zh. Z.,Prokof'eva, A. F.,Koroleva, T. I.,Mel'nikov, N. N.
, p. 205 - 208 (2007/10/02)
The acylation of (2'-hydroxyethyl)amino-1,3,5-triazines with chloroacetyl chloride with subsequent reaction of the resulting (2'-chloroacetoxyethyl)aminotriazines with potassium thiocyanate is described.Acylated derivatives of substituted (2'-aminoethyl)aminotriazines were obtained by the reaction of the chlorotriazines with monoacylethylenediamines.
