114826-86-7 Usage
General Description
(1R, 3S, 4R)-3-Benzyloxy-4-(benzyloxymethyl)cyclopentanamine is a chemical compound that belongs to the class of cyclopentane derivatives. It consists of a cyclopentane ring with a benzyloxy group at the 3rd position and a benzyloxymethyl group at the 4th position, as well as an amine group attached to the 1st position. (1R, 3S, 4R)-3-Benzyloxy-4-(benzyloxymethyl)cyclopentanamine has potential applications in medicinal chemistry, specifically as a building block for the synthesis of complex organic molecules. It may also have biological activity due to its structure, and further research may be warranted to explore its potential uses in pharmaceuticals or other industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 114826-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,8,2 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 114826-86:
(8*1)+(7*1)+(6*4)+(5*8)+(4*2)+(3*6)+(2*8)+(1*6)=127
127 % 10 = 7
So 114826-86-7 is a valid CAS Registry Number.
114826-86-7Relevant articles and documents
CARBOCYCLIC NUCLEOSIDE ANALOGUE
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Page/Page column 11; 13-14, (2020/12/30)
The present invention relates to novel hydrolytically stable carbocyclic 5-aza-2-deoxycytidine and carbocyclic 5-aza-cytidine compounds and prodrugs thereof as hypomethylating agents.
New convergent synthesis of carbocyclic nucleoside analogues
Ludek, Olaf R.,Meier, Chris
, p. 2101 - 2109 (2007/10/03)
Two convergent approaches towards the synthesis of carbocyclic nucleoside analogs will be described. Both approaches start from the stereochemically pure cyclopentenol 8 that has been prepared enantioselectively from an alkylated cyclopentadiene. Using these approaches, carbocyclic analogues of dT, FdU and BVdU have been prepared. Moreover, the conversion into the cycloSalpronucleotide and the corresponding nucleotide will be presented for one example.
