341536-51-4 Usage
Description
(1S,3R,4S,7R)-1-[[(4,4'-dimethoxytrityl)oxy]methyl]-7-hydroxy-3-(6-N-benzoyladenin-9-yl)-2,5-dioxabicyclo[2.2.1]heptane is a complex organic compound characterized by its bicyclic structure. It features a trityl-protected hydroxyl group, a benzoyladenine moiety, and a dioxabicycloheptane core. (1S,3R,4S,7R)-1-[[(4,4'-dimethoxytrityl)oxy]methyl]-7-hydroxy-3-(6-N-benzoyladenin-9-yl)-2,5-dioxabicyclo[2.2.1]heptane is of interest in the fields of organic synthesis and medicinal chemistry due to the presence of functional groups that are commonly utilized in these areas. The specific biological or chemical properties of the compound are contingent upon its intended application and the reactivity of its various components.
Uses
Used in Organic Synthesis:
(1S,3R,4S,7R)-1-[[(4,4'-dimethoxytrityl)oxy]methyl]-7-hydroxy-3-(6-N-benzoyladenin-9-yl)-2,5-dioxabicyclo[2.2.1]heptane serves as a key intermediate in organic synthesis, particularly for the creation of complex molecular structures. Its trityl-protected hydroxyl group and benzoyladenine moiety make it a versatile building block for the development of new organic compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (1S,3R,4S,7R)-1-[[(4,4'-dimethoxytrityl)oxy]methyl]-7-hydroxy-3-(6-N-benzoyladenin-9-yl)-2,5-dioxabicyclo[2.2.1]heptane is used as a precursor for the synthesis of potential pharmaceutical agents. (1S,3R,4S,7R)-1-[[(4,4'-dimethoxytrityl)oxy]methyl]-7-hydroxy-3-(6-N-benzoyladenin-9-yl)-2,5-dioxabicyclo[2.2.1]heptane's unique structure and functional groups can be leveraged to design and develop new drugs with specific therapeutic targets.
Used in Chemical Research:
(1S,3R,4S,7R)-1-[[(4,4'-dimethoxytrityl)oxy]methyl]-7-hydroxy-3-(6-N-benzoyladenin-9-yl)-2,5-dioxabicyclo[2.2.1]heptane is also utilized in chemical research to study the reactivity and properties of its functional groups. Understanding these properties can lead to advancements in synthetic methodologies and the discovery of new chemical reactions.
Used in the Development of Bioactive Molecules:
Due to the presence of a benzoyladenine moiety, which is structurally similar to adenine—a key component of nucleic acids—(1S,3R,4S,7R)-1-[[(4,4'-dimethoxytrityl)oxy]methyl]-7-hydroxy-3-(6-N-benzoyladenin-9-yl)-2,5-dioxabicyclo[2.2.1]heptane can be employed in the development of bioactive molecules with potential applications in molecular biology and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 341536-51-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,1,5,3 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 341536-51:
(8*3)+(7*4)+(6*1)+(5*5)+(4*3)+(3*6)+(2*5)+(1*1)=124
124 % 10 = 4
So 341536-51-4 is a valid CAS Registry Number.
341536-51-4Relevant articles and documents
&α-L-ribo-Configured Locked Nucleic Acid (&α-L-LNA): Synthesis and Properties
Soerensen, Mads D.,Kvaernoe, Lisbet,Bryld, Torsten,Hakansson, Anders E.,Verbeure, Birgit,Gaubert, Gilles,Herdewijn, Piet,Wengel, Jesper
, p. 2164 - 2176 (2007/10/03)
The syntheses of monomeric nucleosides and 3'-O-phosphoramidite building blocks en route to α-L-ribo-configured locked nucleic acids (α-L-LNA), composed entirely of α-L-LNA monomers (α-L-ribo configuration) or of a mixture of α-L-LNA and DNA monomers (β-D
