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2,3-Pyridinedicarboxylic acid, 5-[(4-fluorophenyl)methyl]-, 2-ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

863442-90-4

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863442-90-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 863442-90-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,4,4 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 863442-90:
(8*8)+(7*6)+(6*3)+(5*4)+(4*4)+(3*2)+(2*9)+(1*0)=184
184 % 10 = 4
So 863442-90-4 is a valid CAS Registry Number.

863442-90-4Relevant academic research and scientific papers

HIV INTEGRASE INHIBITORS

-

, (2015/09/22)

The present invention features compounds that are HIV integrase inhibitors and therefore are useful in the inhibition of HIV replication, the prevention and/or treatment of infection by HIV, and in the treatment of AIDS and/or ARC.

Synthesis and antiviral activity of 7-benzyl-4-hydroxy-1,5-naphthyridin- 2(1H)-one HIV integrase inhibitors

Boros, Eric E.,Edwards, Cynthia E.,Foster, Scott A.,Fuji, Masahiro,Fujiwara, Tamio,Garvey, Edward P.,Golden, Pamela L.,Hazen, Richard J.,Jeffrey, Jerry L.,Johns, Brian A.,Kawasuji, Takashi,Kiyama, Ryuichi,Koble, Cecilia S.,Kurose, Noriyuki,Miller, Wayne H.,Mote, Angela L.,Murai, Hitoshi,Sato, Akihiko,Thompson, James B.,Woodward, Mark C.,Yoshinaga, Tomokazu

experimental part, p. 2754 - 2761 (2010/01/16)

The medicinal chemistry and structure-activity relationships for a novel series of 7-benzyl-4-hydroxy-1,5-naphthyridin-2(1H)-one HIV-integrase inhibitors are disclosed. Substituent effects were evaluated at the N-1, C-3, and 7-benzyl positions of the naph

A scaleable synthesis of methyl 3-amino-5-(4-fluorobenzyl)-2- pyridinecarboxylate

Boros, Eric E.,Burova, Svetlana A.,Erickson, Greg A.,Johns, Brian A.,Koble, Cecilia S.,Kurose, Noriyuki,Sharp, Matthew J.,Tabet, Elie A.,Thompson, James B.,Toczko, Matthew A.

, p. 899 - 902 (2012/12/30)

A scaleable synthesis of methyl 3-amino-5-(4-fluorobenzyl)-2- pyridinecarboxylate (1b), starting from 5-bromo-2-methoxypyridine (8) and 4-fluorobenzaldehyde (9), is described. Key steps in the process include lithium-bromine exchange of 8, addition of the

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