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1-{(2R,4S,5R)-5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-tetrahydro-thiophen-2-yl}-5-methyl-1H-pyrimidine-2,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

151607-33-9

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151607-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151607-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,6,0 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 151607-33:
(8*1)+(7*5)+(6*1)+(5*6)+(4*0)+(3*7)+(2*3)+(1*3)=109
109 % 10 = 9
So 151607-33-9 is a valid CAS Registry Number.

151607-33-9Relevant academic research and scientific papers

The chemical synthesis and X-ray structure of the sulfone of 4'-thiothymidine

Hancox,Hamor,Walker

, p. 1291 - 1294 (1994)

Oxidation of 4'-thiothymidine with MCPBA results in its smooth conversion in high yield to the corresponding sulfone. The X-ray structure of this novel analogue showed that the sugar ring has a very similar conformation (C2'-endo, C3'-endo, S) to that fou

Amplification of 4′-thioDNA in the presence of 4′-thio-dTTP and 4′-thio-dCTP, and 4′-thioDNA-directed transcription in vitro and in mammalian cells

Inoue, Naonori,Shionoya, Aki,Minakawa, Noriaki,Kawakami, Akiko,Ogawa, Naoki,Matsuda, Akira

, p. 15424 - 15425 (2007)

Herein we describe the synthesis of 4′-thio-dTTP (1) and 4′-thio-dCTP (2) and their susceptibility for PCR amplification. Double stranded 4′-thioDNAs were amplified sufficiently by KOD dash DNA polymerase under appropriate conditions. Through this PCR stu

Compounds and oligomeric compounds comprising novel nucleobases

-

Page/Page column 58;-60, (2008/06/13)

The present invention relates to nucleoside compositions comprising novel nucleobases and oligomeric compounds comprising at least one such nucleoside. These oligomeric compounds typically have enhanced binding affinity properties compared to oligomeric compounds without the modification. The oligomeric compounds are useful, for example, for investigative and therapeutic purposes.

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