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N6-benzoyl-9-(3',5'-di-O-methylsulfonyl-2'-deoxy-β-D-threo-pentofuranosyl)adenine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

606141-35-9

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606141-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 606141-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,6,1,4 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 606141-35:
(8*6)+(7*0)+(6*6)+(5*1)+(4*4)+(3*1)+(2*3)+(1*5)=119
119 % 10 = 9
So 606141-35-9 is a valid CAS Registry Number.

606141-35-9Relevant academic research and scientific papers

Study on disulfur-backboned nucleic acid: Part 1, efficient synthesis of 3′,5′-dithio-2′-deoxyadenosine

Zheng, Hongchao,Cheng, Changmei,Wang, Hua,Xu, Shanshan,Zhao, Yufen

, p. 2585 - 2587 (2007/10/03)

An efficient procedure is established to synthesize 3′,5′- dithio-2′-deoxyadenosine starting from 2′-deoxyadenosine in five steps in 33% overall yield. In this procedure, the key intermediate 9 was synthesized by twice SN2 reactions with twice

Deoxynucleic guanidine: Synthesis and incorporation of purine nucleosides into positively charged DNG oligonucleotides

Challa, Hemavathi,Bruice, Thomas C.

, p. 1475 - 1481 (2007/10/03)

The synthesis of purine nucleosides capable of making the guanidinium linkage is described for the first time starting from the corresponding 2′-deoxynucleosides. The positively charged mixed base DNG oligomer containing guanine was synthesized on solid-p

Novel and efficient syntheses of 3′,5′-diamino derivatives of 2′,3′,5′-trideoxycytidine and 2′,3′,5′-trideoxyadenosine. Protonation behavior of 3′,5′-diaminonucleosides

Lavandera, Iván,Fernández, Susana,Ferrero, Miguel,Gotor, Vicente

, p. 5449 - 5456 (2007/10/03)

High yielding synthetic routes to 3′,5′-diamino-2′,3′,5′-trideoxycytidine and 3′,5′-diamino-2′,3′,5′-trideoxyadenosine are described. In addition, the protonation behavior of 3′,5′-diamino-2′,3′,5′-trideoxycytidine, 3′,5′-diamino-2′,3′,5′-trideoxyadenosin

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