4814-81-7 Usage
Uses
Used in Pharmaceutical Industry:
Acetamide, N-[2-(methylamino)ethyl]is used as a pharmaceutical intermediate for the synthesis of various drugs and medications. Its unique chemical structure allows it to serve as a building block in the development of new pharmaceutical compounds, contributing to the advancement of medical treatments.
Used in Pesticide Manufacturing:
Acetamide, N-[2-(methylamino)ethyl]is utilized in the production of pesticides, where it plays a crucial role in the formulation of effective and targeted pest control solutions. Its chemical properties enable it to be incorporated into various pesticide formulations, enhancing their efficacy and performance.
Used in Dye Production:
Acetamide, N-[2-(methylamino)ethyl]is employed in the manufacturing of dyes, where it contributes to the creation of a diverse range of colorants for various applications. Its chemical properties allow it to be integrated into dye formulations, resulting in vibrant and stable colorants.
Used in Organic Compound Synthesis:
This versatile chemical is used in the synthesis of other organic compounds, serving as a key component in the production of various chemical products. Its reactivity and compatibility with other chemicals make it a valuable asset in the synthesis of a wide array of organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 4814-81-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,1 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4814-81:
(6*4)+(5*8)+(4*1)+(3*4)+(2*8)+(1*1)=97
97 % 10 = 7
So 4814-81-7 is a valid CAS Registry Number.
4814-81-7Relevant academic research and scientific papers
Yokoyama, Soichi,Shibauchi, Hiroshi,Asahara, Haruyasu,Nishiwaki, Nagatoshi
, p. 1125 - 1133 (2019)
Efficient α-aryl-β-keto ester acylation of amine accompanied by the elimination of ethyl phenylacetate was achieved owing to the pseudo-intramolecular process. The eliminated ethyl phenylacetate could be recycled by conversion into an α-aryl-β-keto ester upon treatment with an acyl chloride in the presence of lithium bis(trimethylsilyl)amide, by which the atom economy considerably increased. Acylation using an α-aryl-β-keto ester is highly sensitive to the bulkiness of the nucleophile, which facilitated the regioselective-acylation of the less hindered amino group in diamine without protecting the other. The transacylation of α-aryl-β-keto ester with N-alkylamino alcohol resulted in chemoselective O-acylation without protecting the amino group because the hydroxy group was attracted to the reaction site of the keto ester by forming an ammonium salt. Transacylation was demonstrated to be a practically useful tool for organic synthesis because this protocol can be conducted under mild conditions with simple manipulations in the absence of any additives such as metal catalyst and base.
