137706-80-0

Basic information

• Product Name: Acetamide, N-acetyl-N-[2-(acetylamino)ethyl]-
• Synonyms: Acetamide, N-acetyl-N-[2-(acetylamino)ethyl]-
• CAS NO: 137706-80-0
• Molecular Formula: C₈H₁₄N₂O₃
• Molecular Weight: 186.21
• Mol File: 137706-80-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Acetamide, N-acetyl-N-[2-(acetylamino)ethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, N-acetyl-N-[2-(acetylamino)ethyl]-(137706-80-0)
• EPA Substance Registry System: Acetamide, N-acetyl-N-[2-(acetylamino)ethyl]-(137706-80-0)

Safety Data

• Hazardous Substances Data: 137706-80-0(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
Acetamide, N-acetyl-N-[2-(acetylamino)ethyl]is used as a reagent in organic synthesis for the preparation of various complex organic molecules. Its unique structure allows it to be a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research and Development:
Acetamide, N-acetyl-N-[2-(acetylamino)ethyl]is used as a research compound in academic and industrial laboratories. It serves as a model compound for studying the properties and reactivity of carboximidic acids and their derivatives, contributing to the advancement of organic chemistry and related fields.
Note: Since the provided materials do not mention specific applications in different industries, the uses are generalized based on the information available. Further research may reveal additional applications and industries where this compound is utilized.

Upstream product

• 10543-57-4 N,N,N',N'-tetraacetylethylenediamine 
• 871-78-3 N,N'-diacetylethylenediamine 
• 108-24-7 acetic anhydride 
• 64-19-7 acetic acid 

Downstream Products

• 79-21-0 peracetic acid 
• 871-78-3 N,N'-diacetylethylenediamine 
• 64-19-7 acetic acid 
• 10543-57-4 N,N,N',N'-tetraacetylethylenediamine 
• 108-24-7 acetic anhydride 

Relevant articles and documents

Degradation and photodegradation of tetraacetylethylenediamine (TAED) in the presence of iron (III) in aqueous solution

The dark degradation of tetraacetylethylenediamine (TAED) was investigated, It is a slow process which is favored in acidic medium, There is a hydrolysis of an imide group with the scission of the C-N bond giving rise to the triacetyl derivative (TAED'). When allowed to stand for longer times a second acetyl group is eliminated with the formation of the symetric diacetyl derivative (DAED). The degradation of TAED photoinduced by iron (m) was also investigated. It appears a faster degradation which does not lead to the same products. The process only involves 'OH radicals formed upon photolysis of aquocomplex of iron (III). They preferentially abstract a hydrogen from the methylene group. The degradation is then assisted by oxygen and leads to the formation of carbonylated oxidation products.

Three of a kind of high purity process for the preparation of acetyl ethylenediamine

the invention belongs to the technical field of preparation method of amide compounds in organic chemistry, and particularly relates to a preparation method of high purity triacetyl ethylene diamine. The method comprises the following steps: a, adding diacetyl ethylenediamine and acetic anhydride into a reaction vessel; b, heating for reaction at the temperature of 100-140 DEG C; c, cooling for crystallization and filtering solid products to obtain a filtrate; d, concentrating and crystallizing the filtrate to obtain a triacetyl ethylene diamine crude product; e, adding a solvent into the crude product and carrying out recrystallization for purification; and f, filtering, washing and drying to obtain a triacetyl ethylene diamine pure product. The method provided by the invention has simple technological process, can prepare high purity triacetyl ethylene diamine, which is used as a standard sample to meet the establishment of a gas phase detection method, and has extremely vital significance to TAED synthesis study and application mechanism research.

Kinetic model of acylation of diacetylethylenediamine

Descriptive kinetics of synthesis of tetraacetylethylenediamine by acylation of diacetylethylenediamine with acetic acid anhydride was examined. The apparent rate constants of the process were obtained, and a mathematical model adequately describing the process was constructed.

Kinetics of the Hydrolysis and Perhydrolysis of Tetraacetylethylenediamine, a Peroxide Bleach Activator

Hydrogen peroxide and water react with tetraacetylethylenediamine (TAED) to form consecutively triacetylethylenediamine and diacetylethylenediamine with the release of two molecules of peracetic acid or acetic acid.The effect of pH, specific buffers and temperature on the rates of hydrolysis and perhydrolysis are compared.Peracetic acid reacts with TAED very slowly.The ratio of the second-order rate constants for the reaction of TAED with hydroperoxide and peracetate anions is exceptionally large after taking into account the difference in pKa values of their conjugate acids.The relative reactivity of various nucleophiles with TAED is discussed in terms of its performance as a bleach activator.