59696-82-1 Usage
Uses
Used in Pharmaceutical Industry:
[5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]acetonitrile (non-preferred name) is used as a key intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and functional groups make it a promising candidate for the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Organic Synthesis:
In the field of organic synthesis, [5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]acetonitrile (non-preferred name) serves as a valuable building block for the creation of more complex molecules. Its functional groups can be further modified or reacted to produce a wide range of organic compounds with diverse applications, including materials science, agrochemicals, and specialty chemicals.
Further research and analysis are necessary to fully comprehend the properties and potential applications of [5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]acetonitrile (non-preferred name), as its complex name reflects its specific molecular arrangement. A shortened name could improve clarity and communication about its properties and uses, facilitating its integration into various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 59696-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,9 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59696-82:
(7*5)+(6*9)+(5*6)+(4*9)+(3*6)+(2*8)+(1*2)=191
191 % 10 = 1
So 59696-82-1 is a valid CAS Registry Number.
59696-82-1Relevant academic research and scientific papers
Synthesis and Properties of 5'-Deoxynucleoside 5'-Carboxylic Acids and Derivatives
Meyer, Wilfried,Frollmann, Hartmut
, p. 2530 - 2544 (2007/10/02)
A preparative route to 5'-deoxynucleosid-5'-carbonitriles (3), both of the ribose and deoxyribose series, involves crown ether-catalyzed reaction of nucleoside 5'-tosylates with solid potassium cyanide in organic solvents.O2,5'-Cyclo derivatives of pyrimidine nucleosides can also serve as starting materials.The nitriles 3 require acidic conditions for conversion to the esters 6 of 5'-deoxynucleoside 5'-carboxylic acids (7) which are suitable nucleotide models for biochemical studies.In alkaline solutions compounds 3 undergo rapid elimination of the purine or pyrimidine base.Furthermore the adenine derivative 3a, under addition of the unsaturated sugar fragment 10 yields a new nucleoside 12 in which N6 is inserted in a pyrrolidine ring.The circular dichroism spectra of the new compounds reflect strong electronic interaction between polar C-5'-substituents and the chromophores and are in line with those of other C-5'-modified nucleosides.
