15568-88-4 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
Meldrum's acid is used as a building block for the synthesis of various pharmaceuticals and agrochemicals due to its ability to form stable intermediates and facilitate the creation of complex molecular structures.
Used in Heterocyclic Compound Synthesis:
Meldrum's acid is used as a precursor in the synthesis of heterocyclic compounds, which are important in the development of new drugs and agrochemicals, as well as in materials science for their unique properties.
Used in Organic Synthesis as a Reagent:
Meldrum's acid is utilized as a reagent in the preparation of esters and amides, contributing to the formation of various organic compounds with diverse applications in chemical research and industry.
Used in Materials Science:
Meldrum's acid has potential applications in materials science, where its unique chemical properties can be leveraged to develop new materials with specific characteristics for various uses.
Used in Drug Discovery:
Meldrum's acid is employed in drug discovery processes, where its reactivity and ability to form stable intermediates can aid in the development of novel therapeutic agents with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 15568-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,6 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15568-88:
(7*1)+(6*5)+(5*5)+(4*6)+(3*8)+(2*8)+(1*8)=134
134 % 10 = 4
So 15568-88-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO4/c1-7(2)11-5(9)4(3-8)6(10)12-7/h3-4,8H,1-2H3/b8-3+
15568-88-4Relevant academic research and scientific papers
Synthesis of Indeno4,6>thiadiazines from S,S-Dialkylsulfur Diimides
Ried, Walter,Jacobi, Markus A.
, p. 805 - 808 (2007/10/02)
Reaction of S,S-dialkylsulfur diimides 1a-f with (alkoxyalkyliden)-1,3-indanediones and similar compounds 2a-g leads to N-monosubstituted dialkyl sulfur diimides 3a-v.From these 3c-e,k,l can be cyclized to indeno4,6>thiadiazines 4a-
