28860-25-5 Usage
Description
N-ethyl-N-methyl-Formamide, with the chemical formula C5H11NO, is a derivative of formamide. It is a chemical compound that is commonly used as a solvent in various industrial processes and chemical reactions.
Uses
Used in Chemical Industry:
N-ethyl-N-methyl-Formamide is used as a solvent for facilitating various chemical reactions and processes. Its solvent properties make it a valuable component in the chemical industry.
Used in Industrial Processes:
N-ethyl-N-methyl-Formamide is utilized in different industrial processes due to its ability to dissolve a wide range of substances. This makes it a versatile compound for numerous applications within the industry.
However, it is important to note that N-ethyl-N-methyl-Formamide is considered a hazardous material. Exposure to it can cause irritation to the skin, eyes, and respiratory system. It is also harmful if ingested, inhaled, or absorbed through the skin, and it may have harmful effects on the liver and kidneys. Therefore, proper safety measures and protective equipment should be used when handling this chemical to minimize potential health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 28860-25-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,8,6 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 28860-25:
(7*2)+(6*8)+(5*8)+(4*6)+(3*0)+(2*2)+(1*5)=135
135 % 10 = 5
So 28860-25-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H9NO/c1-3-5(2)4-6/h4H,3H2,1-2H3
28860-25-5Relevant articles and documents
Cationic Carbon to Nitrogen Rearrangements in the Reactions of N-(Sulfonyloxy)amines with Aldehydes
Hoffman, Robert V.,Salvador, James M.
, p. 4487 - 4490 (2007/10/02)
A series of aromatic and aliphatic aldehydes was reacted with N-((p-nitrobenzenesulfonyl)oxy)methylamine in chloroform.Products resulting from both carbon migration and hydride migration to nitrogen were isolated.The ratios of carbon to hydride migration products were used to clarify the reaction mechanism.The results support a two-step process in which cationic carbon to nitrogen rearrangements is rate determining.
