81758-54-5 Usage
Uses
Used in Organic Synthesis:
(3,4-dioxo-2-phenylcyclobut-1-en-1-yl)methyl acetate serves as a crucial building block in organic synthesis, contributing to the creation of a wide array of chemical products. Its versatility in reactions allows for the development of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (3,4-dioxo-2-phenylcyclobut-1-en-1-yl)methyl acetate is utilized as a key intermediate for the synthesis of various drugs. Its unique structure plays a vital role in the development of new medicinal compounds with potential therapeutic benefits.
Used in Agrochemical Production:
(3,4-dioxo-2-phenylcyclobut-1-en-1-yl)methyl acetate also finds application in the agrochemical sector, where it is employed as a building block for the synthesis of different agrochemicals. Its use in this industry helps in the development of products aimed at enhancing agricultural productivity.
Used as a Flavoring Ingredient in Food Products:
(3,4-dioxo-2-phenylcyclobut-1-en-1-yl)methyl acetate extends its utility to the food industry, where it is used as a flavoring ingredient. Its distinctive properties allow it to contribute to the taste and aroma profiles of various food products.
Used in the Development of New Drugs and Materials:
Owing to its unique chemical structure and reactivity, (3,4-dioxo-2-phenylcyclobut-1-en-1-yl)methyl acetate holds potential in the research and development of innovative drugs and materials. Its application in this domain facilitates the exploration of novel therapeutic agents and advanced material technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 81758-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,7,5 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81758-54:
(7*8)+(6*1)+(5*7)+(4*5)+(3*8)+(2*5)+(1*4)=155
155 % 10 = 5
So 81758-54-5 is a valid CAS Registry Number.
81758-54-5Relevant academic research and scientific papers
Reactions of Cyclobutenediones, LXII. - 3-(α-Bromoalkyl)-4-phenylcyclobutene-1,2-diones
Ried, Walter,Vogl, Manfred,Knorr, Harald
, p. 396 - 405 (2007/10/02)
Bromination of 3-alkyl-4-phenylcyclobutene-1,2-dione 1a-c leads to the title compounds 2a-c and 4 which react with C, O, and S nucleophiles to yield the substitution products 3a-r, 5a, and 5b.Hydrolysis of the acylal 5a furnishes the ring enlarged structure 7.With hydrogen sulfide 2a, b are converted into the dispiro compounds 9a, b.Reaction of 2a with the thiocarbonyl compounds 11a-d affords the salts 12a-d from which 12c and 12d can be degraded to give the (β-anilinoalkenyl)cyclobutenediones 13a and b.
