5406-65-5 Usage
Uses
Used in Pharmaceutical Synthesis:
Ethyl 5-(chloromethyl)-2-oxotetrahydrofuran-3-carboxylate is used as an intermediate in the synthesis of pharmaceuticals. Its reactive chloromethyl group allows for various organic reactions, making it a valuable component in the development of new drugs.
Used in Agrochemical Synthesis:
Ethyl 5-(chloromethyl)-2-oxotetrahydrofuran-3-carboxylate is also used as an intermediate in the synthesis of agrochemicals. Its reactivity and versatility in organic reactions contribute to the creation of effective agricultural products.
Used in Organic Synthesis:
As a reagent in organic synthesis, ethyl 5-(chloromethyl)-2-oxotetrahydrofuran-3-carboxylate is used for various chemical reactions. Its chloromethyl group makes it a useful building block for the synthesis of complex organic compounds.
Used in Research and Development:
Ethyl 5-(chloromethyl)-2-oxotetrahydrofuran-3-carboxylate is utilized in research and development for the exploration of new chemical reactions and the creation of novel compounds. Its unique properties make it an essential tool in advancing the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 5406-65-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5406-65:
(6*5)+(5*4)+(4*0)+(3*6)+(2*6)+(1*5)=85
85 % 10 = 5
So 5406-65-5 is a valid CAS Registry Number.
5406-65-5Relevant academic research and scientific papers
Five membered ring formation of 2-hydroxyalkyl malonate and acetoacetate derivatives the problem of O-versus C-alkylation
Adams, Elisabeth,Hiegemann, Monika,Duddeck, Helmut,Welzel, Peter
, p. 5975 - 5992 (2007/10/02)
The cyclization reactions of type 32, 34, 36, 37/38 compounds have been studied with the aim of achieving a carbon-carbon bond forming reaction at C-2 of optically active glycerol derivatives as indicated in Scheme 1. In all cases O-alkylation at the proximal CO group has been observed.
