Cas 174074-51-2,1-<2,3-dideoxy-3-ethynyl-5-O-(triphenylmethyl)-β-D-ribofuranosyl>pyrimidine-2,4(1H,3H)-dione

174074-51-2

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Basic information

Product Name: 1-<2,3-dideoxy-3-ethynyl-5-O-(triphenylmethyl)-β-D-ribofuranosyl>pyrimidine-2,4(1H,3H)-dione
Synonyms: 1-<2,3-dideoxy-3-ethynyl-5-O-(triphenylmethyl)-β-D-ribofuranosyl>pyrimidine-2,4(1H,3H)-dione
CAS NO:174074-51-2
Molecular Formula:
Molecular Weight: 478.547
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-<2,3-dideoxy-3-ethynyl-5-O-(triphenylmethyl)-β-D-ribofuranosyl>pyrimidine-2,4(1H,3H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: 1-<2,3-dideoxy-3-ethynyl-5-O-(triphenylmethyl)-β-D-ribofuranosyl>pyrimidine-2,4(1H,3H)-dione(174074-51-2)
EPA Substance Registry System: 1-<2,3-dideoxy-3-ethynyl-5-O-(triphenylmethyl)-β-D-ribofuranosyl>pyrimidine-2,4(1H,3H)-dione(174074-51-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 174074-51-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 174074-51-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,0,7 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 174074-51:
(8*1)+(7*7)+(6*4)+(5*0)+(4*7)+(3*4)+(2*5)+(1*1)=132
132 % 10 = 2
So 174074-51-2 is a valid CAS Registry Number.

174074-51-2Upstream product

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174074-51-2Relevant academic research and scientific papers

3',4'-diethynyl-2',3',5'-trideoxy-5'-noruridine: A new self-polymerizable 2'-deoxyribonucleoside analogue

Amin,Stoeckli-Evans,Gossauer

, p. 1879 - 1886 (2007/10/02)

In 10 steps, 3',4'-diethynyl-2',3',5'-trideoxy-5'-noruridine (14) was synthesized in 5% overall yield from commercial uridine, using conventional methods of nucleoside chemistry. As two functional groups capable to react with each other are present in the

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