169287-67-6 Usage
Chemical compound
2-Amino-6-chloro-9H-purine-9-acetic acid benzyl ester
Commonly used in
Organic synthesis and pharmaceutical research
Derivative of
2-amino-6-chloropurine
Type of compound
Purine analog
Known for potential as
Building block in the synthesis of nucleoside analogs
Importance in
Development of antiviral and anticancer drugs
Studied for potential as
G-quadruplex DNA ligand
Relevance in
Cancer treatment
Investigated for potential as
Inhibitor of cAMP-specific phosphodiesterases
Involvement in
Various signaling pathways in the body
Overall
Versatile and important chemical compound with various potential applications in medicine and organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 169287-67-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,2,8 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 169287-67:
(8*1)+(7*6)+(6*9)+(5*2)+(4*8)+(3*7)+(2*6)+(1*7)=186
186 % 10 = 6
So 169287-67-6 is a valid CAS Registry Number.
169287-67-6Relevant articles and documents
Expanding the scope and orthogonality of PNA synthesis
Pothukanuri, Srinivasu,Pianowski, Zbigniew,Winssinger, Nicolas
supporting information; experimental part, p. 3141 - 3148 (2009/05/27)
Peptide nucleic acids (PNAs) hybridize to natural oligonucleotides according to Watson and Crick base-pairing rules. The robustness of PNA oligomers and ease of synthesis have made them an attractive platform to encode small or macromolecules for microarr
Synthesis of modified diaminopurines and their incorporation into oligomers
-
, (2008/06/13)
Protected diaminopurines can be used in the synthesis of nucleic acid binding compounds containing diaminepurine in place of other nucleobases. A method for the synthesis of protected diaminopurines is disclosed which is convenient for incorporating modif
