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1H-Purine, 2-fluoro-6-(phenylmethoxy)-, also known as 2-fluoro-6-(phenylmethoxy)purine, is a chemical compound belonging to the purine family. It is characterized by a purine core structure, with a fluorine atom at the 2-position and a phenylmethoxy group attached at the 6-position. 1H-Purine, 2-fluoro-6-(phenylmethoxy)- is of interest in medicinal chemistry and drug development due to its potential biological activities and its ability to modulate various biochemical pathways. The specific substitution of fluorine and phenylmethoxy groups can significantly influence the compound's reactivity, stability, and interaction with biological targets, making it a subject of study for the development of new therapeutic agents.

19916-74-6

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19916-74-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19916-74-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,1 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19916-74:
(7*1)+(6*9)+(5*9)+(4*1)+(3*6)+(2*7)+(1*4)=146
146 % 10 = 6
So 19916-74-6 is a valid CAS Registry Number.

19916-74-6Upstream product

19916-74-6Downstream Products

19916-74-6Relevant academic research and scientific papers

Purine-Derived Nitroxides for Noncovalent Spin-Labeling of Abasic Sites in Duplex Nucleic Acids

Kamble, Nilesh R.,Sigurdsson, Snorri Th.

, p. 4157 - 4164 (2018)

A series of purine-based spin labels was prepared for noncovalent spin-labeling of abasic sites of duplex nucleic acids through hydrogen bonding to an orphan base on the opposing strand and π-stacking interactions with the flanking bases. Both 1,1,3,3-tet

8-substituted O6-benzylguanine, substituted 6(4)-(benzyloxy)pyrimidine, and related derivatives as inactivators of human O6-alkylguanine-DNA alkyltransferase

Chae,Swenn,Kanugula,Dolan,Pegg,Moschel

, p. 359 - 365 (2007/10/02)

Several 8-substituted O6-benzylguanines, 2- and/or 8-substituted 6- (benzyloxy)purines, substituted 6(4)-(benzyloxy)pyrimidines, and a 6- (benzyloxy)-s-triazine were tested for their ability to inactivate the human DNA repair protein, O6/

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