89760-74-7 Usage
Description
1-(6-amino-9H-purin-9-yl)-3-(prop-2-en-1-yloxy)propan-2-ol is a chemical compound that features a purine molecule with a six-membered ring composed of four nitrogen atoms and two carbon atoms. 1-(6-amino-9H-purin-9-yl)-3-(prop-2-en-1-yloxy)propan-2-ol also includes a propanol group, which is made up of three carbon atoms and a hydroxyl group. Furthermore, it has a propen-1-yloxy group connected to the propanol group, characterized by a double bond between two carbon atoms and an oxygen atom. Structurally related to nucleotides and nucleosides, which play a crucial role in DNA and RNA synthesis, this compound may hold potential applications in the fields of pharmaceuticals and biochemistry due to its unique structural properties.
Uses
Used in Pharmaceutical Industry:
1-(6-amino-9H-purin-9-yl)-3-(prop-2-en-1-yloxy)propan-2-ol is used as a potential therapeutic agent for [application reason] due to its structural resemblance to nucleotides and nucleosides, which are essential in DNA and RNA synthesis.
Used in Biochemical Research:
In the field of biochemistry, 1-(6-amino-9H-purin-9-yl)-3-(prop-2-en-1-yloxy)propan-2-ol serves as a valuable compound for [application reason], possibly contributing to the understanding of nucleotide and nucleoside interactions and their roles in cellular processes.
Check Digit Verification of cas no
The CAS Registry Mumber 89760-74-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,6 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89760-74:
(7*8)+(6*9)+(5*7)+(4*6)+(3*0)+(2*7)+(1*4)=187
187 % 10 = 7
So 89760-74-7 is a valid CAS Registry Number.
89760-74-7Relevant articles and documents
Synthesis of unsaturated adenine derivatives, potential inhibitors of S-adenosyl-L-homocysteine hydrolase
Ozerov,Novikov
, p. 712 - 715 (1996)
The synthesis of 9-substituted adenine derivatives, containing an unsaturated fragment at the end of the acyclic chain, is described; it consists of the alkylation of adenine salts with unsaturated α-haloethers, tosylates, and epoxides. It was shown that compounds of this series possess moderate antiviral activity. 1997 Plenum Publishing Corporation.
