17405-22-0 Usage
Structure
Six-membered nitrogen-containing ring with a hydroxyl group attached to the sixth carbon atom
Derivative
Purine base, commonly found in nucleic acids such as DNA and RNA
Biochemical processes
Involved in various processes in living organisms, plays a crucial role in the synthesis of nucleotides and nucleic acids
Pharmaceutical applications
Potential anti-inflammatory and immunomodulatory properties, currently being studied.
Check Digit Verification of cas no
The CAS Registry Mumber 17405-22-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,0 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17405-22:
(7*1)+(6*7)+(5*4)+(4*0)+(3*5)+(2*2)+(1*2)=90
90 % 10 = 0
So 17405-22-0 is a valid CAS Registry Number.
17405-22-0Relevant academic research and scientific papers
Synthesis of 2-substituted 6-(hydroxymethyl)purine bases and nucleosides
Silhar, Peter,Pohl, Radek,Votruba, Ivan,Hocek, Michal
, p. 1669 - 1695 (2007/10/03)
A facile and efficient methodology of the synthesis of 6-(hydroxymethyl) purine derivatives (bases and nucleosides) was developed based on Pd-catalyzed cross-coupling reactions of 6-halopurines or N-protected 2-amino-6-halopurines with (benzoyloxymethyl)z
Facile and efficient synthesis of 6-(hydroxymethyl)purines
Silhar, Peter,Pohl, Radek,Votruba, Ivan,Hocek, Michal
, p. 3225 - 3228 (2007/10/03)
(Chemical Equation Presented) A facile and efficient methodology of the synthesis of 6-(hydroxymethyl)purine derivatives (bases and nucleosides) was developed based on Pd-catalyzed cross-coupling reactions of 6-halopurines with acyloxymethylzinc iodides f
