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1-(5-O-tert-butyldimethylsilyl-3-O-phenoxythiocarbonyl-2-deoxy-β-D-erythro-pentofuranosyl)-imidazo[4,5-d]pyridazin-4(5H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

260562-60-5

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260562-60-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 260562-60-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,0,5,6 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 260562-60:
(8*2)+(7*6)+(6*0)+(5*5)+(4*6)+(3*2)+(2*6)+(1*0)=125
125 % 10 = 5
So 260562-60-5 is a valid CAS Registry Number.

260562-60-5Downstream Products

260562-60-5Relevant academic research and scientific papers

Synthesis and anti-HIV evaluation of 2',3'-dideoxy imidazo- and ν- triazolo[4,5-d]pyridazine nucleosides

Bussolari, Jacqueline C.,Panzica, Raymond P.

, p. 2373 - 2379 (1999)

The syntheses of the 2'-deoxy and 2',3'-dideoxynucleosides of 2,8-diaza- 3-deazainosine and the 2',3'-dideoxynucleoside of 2-aza-3-deazainosine were achieved and the pathways leading to these novel nucleosides are described. The preparation of the 2',3'-dideoxynucleoside (1) of 2-aza-3-deazainosine involved deoxygenation of the 2'-deoxy-3'-imidazolide intermediate with n- Bu3SnH and AIBN. The latter nucleoside was synthesized from the known 2'- deoxy derivative of 2-aza-3-deazainosine. The three-step synthesis of 1 from the 2'-deoxy analogue was accomplished in 40% overall yield. Rather than synthesize the corresponding 2',3'-dideoxynucleoside (2) of 2,8-diaza-3- deazainosine in the same manner, i.e. deoxygenation of the 2'- deoxynucleoside, a more cost-effective route was chosen. This pathway involved reductive cleavage of the 5'-protected, 2',3'-thiocarbonate derivative to furnish a mixture of the 2'- and 3'-deoxy isomers. This mixture was not separated, but was deoxygenated by the aforementioned imidazolide method. Using this methodology, 2 was prepared in 23% overall yield from 2,8- diaza-3-deazainosine. Nucleosides 1 and 2 were evaluated for antiretroviral activity and were found to be inactive. (C) 1999 Elsevier Science Ltd.

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