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28269-02-5

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28269-02-5 Usage

General Description

The chemical 1,2-Cyclopentanedicarboxylic acid, 4-oxo-, dimethyl ester, (1R,2S)-rel- is a compound with a molecular formula of C9H12O5. It is a dimethyl ester of 1,2-cyclopentanedicarboxylic acid and is also known as (+)-1,2-cyclopentanedicarboxylic acid 4-oxo dimethyl ester. 1,2-Cyclopentanedicarboxylic acid, 4-oxo-, dimethyl ester, (1R,2S)-rel- has potential applications in the fields of medicine, pharmaceuticals, and organic synthesis. It may have properties that make it suitable for use as a building block in the synthesis of various compounds with biological activity. Further research and testing may be required to fully understand the potential uses and implications of this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 28269-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,6 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28269-02:
(7*2)+(6*8)+(5*2)+(4*6)+(3*9)+(2*0)+(1*2)=125
125 % 10 = 5
So 28269-02-5 is a valid CAS Registry Number.

28269-02-5Relevant articles and documents

PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS

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Page/Page column 299-300; 360-362, (2020/10/18)

This disclosure provides pharmaceutical compounds to treat medical disorders, such as complement-mediated disorders, including complement Cl -mediated disorders.

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

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