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Thymidine, 3'-azido-3'-deoxy-, 5'-(4-chlorophenyl phosphonate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

834918-68-2

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834918-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 834918-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,4,9,1 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 834918-68:
(8*8)+(7*3)+(6*4)+(5*9)+(4*1)+(3*8)+(2*6)+(1*8)=202
202 % 10 = 2
So 834918-68-2 is a valid CAS Registry Number.

834918-68-2Relevant academic research and scientific papers

Aryl nucleoside H-phosphonates. Part 16: Synthesis and anti-HIV-1 activity of di-aryl nucleoside phosphotriesters

Romanowska, Joanna,Szymanska-Michalak, Agnieszka,Boryski, Jerzy,Stawinski, Jacek,Kraszewski, Adam,Loddo, Roberta,Sanna, Giuseppina,Collu, Gabriella,Secci, Barbara,Colla, Paolo La

experimental part, p. 3489 - 3498 (2009/09/30)

Di-aryl nucleoside phosphotriesters have been explored as a new type of pronucleotides for the purpose of anti-HIV-1 therapy and efficient synthetic protocols, based on H-phosphonate chemistry, have been developed for the preparation of this class of comp

New and efficient approach to aryl phosphoramidate derivatives of AZT/d4T as anti-HIV prodrugs

Li, Xueshu,Fu, Hua,Jiang, Yuyang,Zhao, Yufen,Liu, Jinyong

, p. 2600 - 2602 (2007/10/03)

Ester exchange of diaryl phosphite with AZT or d4T produced aryl AZT/d4T H-phosphonate, and the following reaction with amino acid esters in the presence of hexachloroethane and triethylamine yielded membrane-soluble anti-HIV prodrugs aryl phosphoramide d

Aryl H-phosphonates. 14. Synthesis of new nucleotide analogues with phosphonate-phosphate internucleosidic linkage

Szymczak, Marzena,Szymanska, Agnieszka,Stawinski, Jacek,Boryski, Jerzy,Kraszewski, Adam

, p. 3571 - 3573 (2007/10/03)

(Equation presented) Aryl nucleoside H-phosphonates 3 and aryl nucleoside P-acylphosphonates 4, generated in situ from the appropriate H-phosphonate 1 and acylphosphonate monoesters 2, respectively, reacted rapidly in the presence of tertiary amines to pr

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