Cas 86132-77-6,3-Amino-4-((3aS,4S,6R,6aR)-2,2-dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-furan-2-carbonitrile

86132-77-6

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Basic information

Product Name: 3-Amino-4-((3aS,4S,6R,6aR)-2,2-dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-furan-2-carbonitrile
Synonyms:
CAS NO:86132-77-6
Molecular Formula:
Molecular Weight: 522.601
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: 3-Amino-4-((3aS,4S,6R,6aR)-2,2-dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-furan-2-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 3-Amino-4-((3aS,4S,6R,6aR)-2,2-dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-furan-2-carbonitrile(86132-77-6)
EPA Substance Registry System: 3-Amino-4-((3aS,4S,6R,6aR)-2,2-dimethyl-6-trityloxymethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl)-furan-2-carbonitrile(86132-77-6)

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: 86132-77-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 86132-77-6 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 86132-77:
(7*8)+(6*6)+(5*1)+(4*3)+(3*2)+(2*7)+(1*7)=136
136 % 10 = 6
So 86132-77-6 is a valid CAS Registry Number.

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86132-77-6Relevant 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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