1001666-74-5 Usage
Description
4-oxo-cyclopentane-cis-1,2-dicarboxylic acid dimethyl ester is an organic compound characterized by the molecular formula C9H14O5. It is a colorless, odorless liquid with a molecular weight of 202.20 g/mol. This dimethyl ester derivative of 4-oxo-cyclopentane-cis-1,2-dicarboxylic acid is frequently utilized as a building block in the synthesis of a variety of other organic compounds, playing a significant role in organic synthesis and as a reagent in chemical reactions.
Uses
Used in Organic Synthesis:
4-oxo-cyclopentane-cis-1,2-dicarboxylic acid dimethyl ester is used as a building block for the synthesis of various organic compounds. Its versatile structure allows it to be a key component in creating a range of molecules with different functional groups and properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-oxo-cyclopentane-cis-1,2-dicarboxylic acid dimethyl ester is used as a reagent in the development of new chemical compounds. Its ability to participate in a wide array of chemical reactions makes it valuable for the synthesis of potential drug candidates and other bioactive molecules.
Used in Research and Development:
4-oxo-cyclopentane-cis-1,2-dicarboxylic acid dimethyl ester is also utilized in research and development settings. It serves as a valuable tool for scientists to explore new reaction pathways, understand the mechanisms of complex chemical transformations, and innovate in the field of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 1001666-74-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,1,6,6 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1001666-74:
(9*1)+(8*0)+(7*0)+(6*1)+(5*6)+(4*6)+(3*6)+(2*7)+(1*4)=105
105 % 10 = 5
So 1001666-74-5 is a valid CAS Registry Number.
1001666-74-5Relevant articles and documents
Enzyme-Catalyzed Asymmetric Synthesis. 8. Enantioselectivity of Pig Liver Esterase Catalyzed Hydrolyses of 4-Substituted Meso Cyclopentane 1,2-Diesters
Gais, Hans-Joachim,Buelow, Gerd,Zatorski, Andrzej,Jentsch, Mathias,Maidonis, Peter,Hemmerle, Horst
, p. 5115 - 5122 (1989)
Hydrolyses of meso-1,2-cyclopentanedicarboxylic acid bis(methyl esters) bearing in the 4-position an oxo, methylene, cis-hydroxy, trans-hydroxy,cis-acetoxy, trans-acetoxy, cis-methoxy, cis-tert-butoxy, ethylenedioxy, propylenedioxy, dimethyl propylenediox
Enantioselective synthesis of an advanced intermediate for the synthesis of brefeldin A and analogues
Legrand, Frédéric,Archambaud, Sylvie,Collet, Sylvain,Aphecetche-Julienne, Karine,Guingant, André,Evain, Michel
, p. 389 - 393 (2008/09/17)
A synthesis of methyl (1R,2R,4S)-2-[(E)-2-iodovinyl]-4-(methoxymethoxy) cyclopentanecarboxylate is described in nine steps from a prochiral anhydride. A desymmetrization reaction followed by an epimerization and a Takai reaction are the key steps of the t
Toward the total synthesis of variecolin
Molander, Gary A.,Quirmbach, Michael S.,Silva Jr., Luiz F.,Spencer, Keith C.,Balsells, Jaume
, p. 2257 - 2260 (2007/10/03)
(matrix presented) An annulative approach toward the total synthesis of the sesterterpenoid variecolin (1) is presented. Synthesis of the key hemiketal, containing the core ABC ring skeleton, has been achieved on a model system by an expeditious route uti
