102539-92-4 Usage
Carboxylic acid derivative
Cyclopentane
A derivative of cyclopentane, which is a five-carbon cyclic hydrocarbon, with a carboxyl functional group (-COOH) attached.
Contains a hydroxymethyl group
A functional group consisting of a hydroxymethyl moiety (-CH2OH) attached to the cyclopentane ring.
Common use in organic synthesis and pharmaceutical research
Widely used as a building block for the production of various pharmaceuticals and agrochemicals due to its versatile chemical structure and reactivity.
Utilized in the synthesis of natural products and heterocyclic compounds
Its unique structure allows it to be used in the creation of complex organic molecules, including natural products and compounds containing a ring structure with at least one non-carbon atom.
Potential applications in drug development and medicinal chemistry
The compound's versatile structure and reactivity make it a valuable resource in the development of new drugs and medicinal compounds, offering a broad range of possibilities for therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 102539-92-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,5,3 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102539-92:
(8*1)+(7*0)+(6*2)+(5*5)+(4*3)+(3*9)+(2*9)+(1*2)=104
104 % 10 = 4
So 102539-92-4 is a valid CAS Registry Number.
102539-92-4Relevant academic research and scientific papers
Selective reductions of cyclic 1,3-diesters by using SmI2 and H2O
Collins, Karl D.,Oliveira, Juliana M.,Guazzelli, Giuditta,Sautier, Brice,De Grazia, Sara,Matsubara, Hiroshi,Helliwell, Madeleine,Procter, David J.
scheme or table, p. 10240 - 10249 (2010/11/18)
SmI2/H2O reduces cyclic 1,3-diesters to 3-hydroxyacids with no over reduction. Furthermore, the reagent system is selective for cyclic 1,3-diesters over acyclic 1,3-diesters, and esters. Radicals formed by one-electron reduction of the ester carbonyl group have been exploited in intramolecular additions to alkenes. The ketal unit and the reaction temperature have a marked impact on the diastereoselectivity of the cyclizations. Cyclization cascades are possible when two alkenes are present in the starting cyclic diester and lead to the formation of two rings and four stereocenters with excellent stereocontrol.
