Cas 160204-60-4,1-(2'-deoxy-2'-phenylselenenyl-3',4',6'-tri-O-acetyl-β-D-gluco-pyranosyl)-uracil

160204-60-4

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Basic information

Product Name: 1-(2'-deoxy-2'-phenylselenenyl-3',4',6'-tri-O-acetyl-β-D-gluco-pyranosyl)-uracil
Synonyms:
CAS NO:160204-60-4
Molecular Formula:
Molecular Weight: 539.401
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'-deoxy-2'-phenylselenenyl-3',4',6'-tri-O-acetyl-β-D-gluco-pyranosyl)-uracil(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2'-deoxy-2'-phenylselenenyl-3',4',6'-tri-O-acetyl-β-D-gluco-pyranosyl)-uracil(160204-60-4)
EPA Substance Registry System: 1-(2'-deoxy-2'-phenylselenenyl-3',4',6'-tri-O-acetyl-β-D-gluco-pyranosyl)-uracil(160204-60-4)

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: 160204-60-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 160204-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,2,0 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 160204-60:
(8*1)+(7*6)+(6*0)+(5*2)+(4*0)+(3*4)+(2*6)+(1*0)=84
84 % 10 = 4
So 160204-60-4 is a valid CAS Registry Number.

160204-60-4Upstream product

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160204-60-4Relevant academic research and scientific papers

Synthesis of 2'-deoxy-pyranosyl nucleosides from glycals through consecutive addition of phenylselenyl chloride and glycosylation. A study of factors controlling the stereoselectivity

El-Laghdach,Matheu,Castillon

, p. 12219 - 12234 (1994)

2'-Deoxy-2'-phenylselenenyl-pyranosyl nucleosides have been synthesized in a stereoselective way starting from glycals using selenium reagents, and converted into 2'-deoxynucleosides by treatment with tributyltin hydride. The stereoselectivity of the reac

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