Cas 86132-79-8,7-((3aS,4S,6R,6aR)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-furo[3,2-d]pyrimidin-4-ylamine

86132-79-8

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Basic information

Product Name: 7-((3aS,4S,6R,6aR)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-furo[3,2-d]pyrimidin-4-ylamine
Synonyms:
CAS NO:86132-79-8
Molecular Formula:
Molecular Weight: 549.626
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-((3aS,4S,6R,6aR)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-furo[3,2-d]pyrimidin-4-ylamine(CAS DataBase Reference)
NIST Chemistry Reference: 7-((3aS,4S,6R,6aR)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-furo[3,2-d]pyrimidin-4-ylamine(86132-79-8)
EPA Substance Registry System: 7-((3aS,4S,6R,6aR)-2,2-Dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-furo[3,2-d]pyrimidin-4-ylamine(86132-79-8)

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: 86132-79-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 86132-79-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,3 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86132-79:
(7*8)+(6*6)+(5*1)+(4*3)+(3*2)+(2*7)+(1*9)=138
138 % 10 = 8
So 86132-79-8 is a valid CAS Registry Number.

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86132-79-8Relevant academic research and scientific papers

SYNTHESIS OF FUROPYRIMIDINE NUCLEOSIDES: A NOVEL C-NUCLEOSIDE ISOSTERE OF ADENOSINE

Bhattacharya, Birendra K.,Lim, Mu-Ill,Otter, Brian A.,Klein, Robert S.

, p. 815 - 818 (2007/10/02)

The synthesis of 4-amino-7-(β-D-ribofuranosyl)-furopyrimidine, a new C-nucleoside analog of adenosine, is described.It involves base-catalyzed cyclization of the 2-(ribofuranosyl)-2-cyano ethers 3 to afford the ribosyl-3-amino-2-cyanofurans 4α and

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