135042-28-3 Usage
General Description
[(2R,4R)-4-(6-amino-9H-purin-9-yl)pyrrolidin-2-yl]methanol is a chemical compound with a molecular structure consisting of a purine ring attached to a pyrrolidin-2-ylmethyl group. The purine ring contains an amino group at the 6th position and a hydroxymethyl group attached to the pyrrolidin-2-yl moiety. [(2R,4R)-4-(6-amino-9H-purin-9-yl)pyrrolidin-2-yl]methanol is a derivative of purine and is commonly used in pharmaceutical research and drug development. It may have potential applications in the treatment of various medical conditions, including cancer and viral infections, due to its structural similarity to nucleic acid bases and potential biological activity. The compound's stereochemistry is defined by the (2R,4R) configuration, which can significantly impact its biological properties and interactions with other molecules. Overall, [(2R,4R)-4-(6-amino-9H-purin-9-yl)pyrrolidin-2-yl]methanol is a chemically and biologically significant compound with potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 135042-28-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,0,4 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 135042-28:
(8*1)+(7*3)+(6*5)+(5*0)+(4*4)+(3*2)+(2*2)+(1*8)=93
93 % 10 = 3
So 135042-28-3 is a valid CAS Registry Number.
135042-28-3Relevant articles and documents
Azadideoxyadenosine: Synthesis, enzymology, and anti-HIV activity
Nishonov, Abdumalik A.,Ma, Xiaohui,Nair, Vasu
, p. 4099 - 4101 (2007/10/03)
Synthesis of an azanucleoside, a new analogue of dideoxyadenosine, is described. This compound is only slowly deaminated by mammalian adenosine deaminase and it is a substrate for adenosine kinase. It exhibits in vitro anti-HIV activity.