54150-57-1 Usage
Description
Acetyl chloride, (benzoyloxy)-, also known as 2-Chloro-2-oxoethyl Benzoate, is an organic compound commonly utilized as a reagent in the synthesis of various chemical compounds. It is characterized by its ability to react with alcohols and sodium azide using triphosgene, making it a versatile component in organic chemistry.
Uses
Used in Organic Synthesis:
Acetyl chloride, (benzoyloxy)is used as a reagent for the organic synthesis of various azidoformates from alcohols and sodium azide, utilizing triphosgene as a catalyst. This application is particularly relevant in the pharmaceutical and chemical industries, where the creation of new compounds is essential for the development of novel drugs and materials.
In the Pharmaceutical Industry:
Acetyl chloride, (benzoyloxy)plays a crucial role in the synthesis of new drug candidates, contributing to the development of innovative treatments for various medical conditions. Its ability to facilitate the formation of azidoformates from alcohols and sodium azide makes it a valuable tool in the design and synthesis of potential therapeutic agents.
In the Chemical Industry:
The use of Acetyl chloride, (benzoyloxy)extends beyond the pharmaceutical sector, as it is also employed in the chemical industry for the production of various materials and compounds. Its versatility as a reagent allows for the creation of a wide range of products, from specialty chemicals to advanced materials with unique properties.
Check Digit Verification of cas no
The CAS Registry Mumber 54150-57-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,5 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54150-57:
(7*5)+(6*4)+(5*1)+(4*5)+(3*0)+(2*5)+(1*7)=101
101 % 10 = 1
So 54150-57-1 is a valid CAS Registry Number.
54150-57-1Relevant articles and documents
Decarboxylative Synthesis of Functionalized Oxindoles via An Iron-Initiated Radical Chain Process and Application in Constructing Diverse Fused-Indoline Heterocycles
Cui, Zhihao,Du, Da-Ming
supporting information, p. 93 - 99 (2017/10/24)
Rapid construction of diverse fused-indoline?heterocycle (FIH) frameworks including high-value pyrroloindolines, furoindolines and thienoindolines in a two-step sequence has been described. The key to success hinges on the adoption of peresters as α-heteroatom alkyl radical precusors, which can smoothly react with N-arylacrylamides via a radical chain process initiated by inexpensive FeCl2?4H2O to afford the functionalized oxindoles, the key intermediates to FIH skeletons. The approach features operationally-simplicity, broad substrates scope and mild conditions. (Figure presented.).
Glycolate ester peracid precursors
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, (2008/06/13)
The invention provides novel bleaching compositions comprising peracid precursors with the general structure STR1 with R, R', R" and L as defined in the specification. Novel peracids and precursors are also herein disclosed. These peracid precursors provide new, proficient and cost-effective compounds for fabric bleaching.
Esters of N,N-Disubstituted 2-Hydroxyacetamides as a Novel Highly Biolabile Prodrug Type for Carboxylic Acid Agents
Bundgaard, Hans,Nielsen, Niels Mork
, p. 451 - 454 (2007/10/02)
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