Cas 67525-72-8,7-((3aR,4R,6R,6aR)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-1,3-dimethyl-3,7-dihydro-purine-2,6-dione

67525-72-8

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Basic information

Product Name: 7-((3aR,4R,6R,6aR)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-1,3-dimethyl-3,7-dihydro-purine-2,6-dione
Synonyms:
CAS NO:67525-72-8
Molecular Formula:
Molecular Weight: 594.667
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: 7-((3aR,4R,6R,6aR)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-1,3-dimethyl-3,7-dihydro-purine-2,6-dione(CAS DataBase Reference)
NIST Chemistry Reference: 7-((3aR,4R,6R,6aR)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-1,3-dimethyl-3,7-dihydro-purine-2,6-dione(67525-72-8)
EPA Substance Registry System: 7-((3aR,4R,6R,6aR)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-1,3-dimethyl-3,7-dihydro-purine-2,6-dione(67525-72-8)

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: 67525-72-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 67525-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,2 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67525-72:
(7*6)+(6*7)+(5*5)+(4*2)+(3*5)+(2*7)+(1*2)=148
148 % 10 = 8
So 67525-72-8 is a valid CAS Registry Number.

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67525-72-8Relevant academic research and scientific papers

STEREOSELECTIVE SYNTHESIS OF α-RIBONUCLEOSIDES FROM 1-HYDROXY SUGARS BY USING 2-FLUOROPYRIDINIUM TOSYLATE

Mukaiyama, Teruaki,Hashimoto, Yukihiko,Hayashi, Yujiro,Shoda, Shin-ichiro

, p. 557 - 560 (2007/10/02)

A novel method for the preparation of α-ribonucleosides was developed by the use of 2-fluoro-1-methylpyridinium tosylate as a condensing reagent.Various α-ribonucleosides were synthesized from 1-hydroxy sugars and trimethylsilylated nitrogen compounds, such as nucleoside bases and azide, in good yields under mild conditions.

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