Cas 160053-58-7,1-<2,3-O-isopropylidene-1-(phenyl)ethynyl-5-O-(p-toluenesulfonyl)-β-D-ribofuranosyl>thymine

160053-58-7

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Basic information

Product Name: 1-<2,3-O-isopropylidene-1-(phenyl)ethynyl-5-O-(p-toluenesulfonyl)-β-D-ribofuranosyl>thymine
Synonyms: 1-<2,3-O-isopropylidene-1-(phenyl)ethynyl-5-O-(p-toluenesulfonyl)-β-D-ribofuranosyl>thymine
CAS NO:160053-58-7
Molecular Formula:
Molecular Weight: 552.605
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-O-isopropylidene-1-(phenyl)ethynyl-5-O-(p-toluenesulfonyl)-β-D-ribofuranosyl>thymine(CAS DataBase Reference)
NIST Chemistry Reference: 1-<2,3-O-isopropylidene-1-(phenyl)ethynyl-5-O-(p-toluenesulfonyl)-β-D-ribofuranosyl>thymine(160053-58-7)
EPA Substance Registry System: 1-<2,3-O-isopropylidene-1-(phenyl)ethynyl-5-O-(p-toluenesulfonyl)-β-D-ribofuranosyl>thymine(160053-58-7)

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: 160053-58-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 160053-58-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,0,5 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 160053-58:
(8*1)+(7*6)+(6*0)+(5*0)+(4*5)+(3*3)+(2*5)+(1*8)=97
97 % 10 = 7
So 160053-58-7 is a valid CAS Registry Number.

160053-58-7Upstream product

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160053-58-7Relevant academic research and scientific papers

A ribonolactone-based approach to the synthesis of 1'-carbon-substituted thymine ribonucleosides

Hayakawa,Miyazawa,Tanaka,Miyasaka

, p. 297 - 308 (2007/10/02)

Thymine ribonucleosides bearing a carbon substituent at the anomeric position were synthesized starting from D-ribonolactone by way of nucleophilic addition reaction of organolithium reagents and subsequent condensation with trimethylsilylated thymine.

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