20308-52-5 Usage
Description
2,2-dichloro-N-(2-ethylhexyl)acetamide, also known as dichloroacetyl-N-(2-ethylhexyl)amine, is a chemical compound that belongs to the class of amides. It is synthesized through the reaction of dichloroacetyl chloride and 2-ethylhexylamine. 2,2-dichloro-N-(2-ethylhexyl)acetamide is recognized for its effectiveness as a corrosion inhibitor in metalworking fluids and lubricants, playing a crucial role in protecting metal surfaces from degradation. However, it is also considered a moderately hazardous substance due to its potential to cause skin and eye irritation, necessitating careful handling, storage, and efforts to minimize environmental exposure to safeguard aquatic organisms and wildlife.
Uses
Used in Metalworking Fluids and Lubricants Industry:
2,2-dichloro-N-(2-ethylhexyl)acetamide is used as a corrosion inhibitor to prevent the degradation of metal surfaces in metalworking fluids and lubricants. Its application is crucial for maintaining the integrity and performance of machinery and equipment in various industrial processes, thereby extending their service life and reducing maintenance costs. 2,2-dichloro-N-(2-ethylhexyl)acetamide's effectiveness in inhibiting corrosion makes it a valuable asset in this industry, despite the need for careful handling and environmental considerations.
Check Digit Verification of cas no
The CAS Registry Mumber 20308-52-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,0 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20308-52:
(7*2)+(6*0)+(5*3)+(4*0)+(3*8)+(2*5)+(1*2)=65
65 % 10 = 5
So 20308-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H19Cl2NO/c1-3-5-6-8(4-2)7-13-10(14)9(11)12/h8-9H,3-7H2,1-2H3,(H,13,14)
20308-52-5Relevant articles and documents
Using N-nitrosodichloroacetamides to conveniently convert linear primary amines into alcohols
Macarthur, Nicholas S.,Wang, Linshu,Mccarthy, Blaine G.,Jakobsche, Charles E.
supporting information, p. 2014 - 2021 (2015/08/18)
The reported rearrangement of N-nitrosodichloroacetamides provides a practicalmethod for converting primary amines into primary alcohols. The reaction sequence is operationally simple, requires only a single purification, and is compatible with a number of common functional groups. Mechanistic studies of the nitrosylation and rearrangement reactions illustrate the increased utility of dichloroacetamides compared to various other amides for this transformation.