75145-82-3 Usage
Uses
Used in Pharmaceutical Industry:
[3,4-dihydroxy-5-(6-oxo-3,6-dihydro-9H-purin-9-yl)tetrahydrofuran-2-yl]acetonitrile (non-preferred name) is used as a potential pharmaceutical compound for its possible biological activities and pharmacological properties. The presence of hydroxy and oxo groups in its structure suggests that it may have applications in drug development, particularly in areas where such functional groups are known to be beneficial.
Used in Research and Development:
In the field of chemical research and development, [3,4-dihydroxy-5-(6-oxo-3,6-dihydro-9H-purin-9-yl)tetrahydrofuran-2-yl]acetonitrile (non-preferred name) serves as a subject of study to understand its potential uses and effects. [3,4-dihydroxy-5-(6-oxo-3,6-dihydro-9H-purin-9-yl)tetrahydrofuran-2-yl]acetonitrile (non-preferred name)'s complex structure and the presence of specific functional groups make it an interesting candidate for exploring new chemical reactions and potential applications in various scientific fields.
Check Digit Verification of cas no
The CAS Registry Mumber 75145-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,4 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 75145-82:
(7*7)+(6*5)+(5*1)+(4*4)+(3*5)+(2*8)+(1*2)=133
133 % 10 = 3
So 75145-82-3 is a valid CAS Registry Number.
75145-82-3Relevant 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.
