![Bicyclo[3.1.0]hexane-1-methanol,4-[2-chloro-6-(methylamino)-9H-purin-9-yl]-2-(phosphonooxy)-,dihyd…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F352134-bicyclo-3-1-0-hexane-1-methanol-4-2-chloro-6-methylamino-9h-purin-9-yl-2-phosphonooxy-dihydrogen-phosphate-ester-1r-2s-4s-5s.webp&w=3840&q=75)
CAS 367909-40-8
:Bicyclo[3.1.0]hexane-1-methanol,4-[2-chloro-6-(methylamino)-9H-purin-9-yl]-2-(phosphonooxy)-,dihydrogen phosphate (ester), (1R,2S,4S,5S)-
Description:
Bicyclo[3.1.0]hexane-1-methanol, 4-[2-chloro-6-(methylamino)-9H-purin-9-yl]-2-(phosphonooxy)-, dihydrogen phosphate (ester), (1R,2S,4S,5S)-, with CAS number 367909-40-8, is a complex organic compound characterized by its bicyclic structure and the presence of a purine derivative. This compound features a bicyclo[3.1.0]hexane framework, which contributes to its unique three-dimensional conformation. The presence of a methanol group and a phosphonooxy group indicates potential reactivity and biological activity, particularly in biochemical pathways involving phosphorylation. The chloro and methylamino substituents on the purine ring suggest that this compound may interact with biological targets, potentially influencing nucleic acid metabolism or signaling pathways. Its stereochemistry, denoted by the (1R,2S,4S,5S) configuration, implies specific spatial arrangements that can affect its biological interactions and pharmacological properties. Overall, this compound may have applications in medicinal chemistry or biochemistry, particularly in the development of therapeutics targeting nucleic acid-related processes.
Formula:C13H18ClN5O8P2
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