114826-86-7 Usage
Description
(1R, 3S, 4R)-3-Benzyloxy-4-(benzyloxymethyl)cyclopentanamine is a cyclopentane derivative featuring a cyclopentane ring with a benzyloxy group at the 3rd position, a benzyloxymethyl group at the 4th position, and an amine group attached to the 1st position. This chemical compound holds potential in medicinal chemistry and may exhibit biological activity due to its unique structure.
Uses
Used in Medicinal Chemistry:
(1R, 3S, 4R)-3-Benzyloxy-4-(benzyloxymethyl)cyclopentanamine is used as a building block for the synthesis of complex organic molecules, particularly in the development of pharmaceuticals. Its unique structure allows for the creation of diverse compounds with potential therapeutic applications.
Used in Pharmaceutical Research:
Due to its potential biological activity, (1R, 3S, 4R)-3-Benzyloxy-4-(benzyloxymethyl)cyclopentanamine is used in pharmaceutical research to explore its possible applications in medicine. Further studies may reveal its efficacy in treating various conditions or diseases, contributing to the advancement of healthcare solutions.
Used in Industrial Applications:
(1R, 3S, 4R)-3-Benzyloxy-4-(benzyloxymethyl)cyclopentanamine may also find use in other industrial applications beyond medicinal chemistry, given its unique chemical properties. Its potential uses could span across different sectors, pending further research and development.
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.
