Cas 1097201-63-2,(3aS,4S,6R,6aR)-6-(acetoxymethyl)-2,2,6a-trimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl 3,5-dinitrobenzoate

1097201-63-2

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Basic information

Product Name: (3aS,4S,6R,6aR)-6-(acetoxymethyl)-2,2,6a-trimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl 3,5-dinitrobenzoate
Synonyms: (3aS,4S,6R,6aR)-6-(acetoxymethyl)-2,2,6a-trimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl 3,5-dinitrobenzoate
CAS NO:1097201-63-2
Molecular Formula:
Molecular Weight: 438.391
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: (3aS,4S,6R,6aR)-6-(acetoxymethyl)-2,2,6a-trimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl 3,5-dinitrobenzoate(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,4S,6R,6aR)-6-(acetoxymethyl)-2,2,6a-trimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl 3,5-dinitrobenzoate(1097201-63-2)
EPA Substance Registry System: (3aS,4S,6R,6aR)-6-(acetoxymethyl)-2,2,6a-trimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl 3,5-dinitrobenzoate(1097201-63-2)

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: 1097201-63-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1097201-63-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,7,2,0 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1097201-63:
(9*1)+(8*0)+(7*9)+(6*7)+(5*2)+(4*0)+(3*1)+(2*6)+(1*3)=142
142 % 10 = 2
So 1097201-63-2 is a valid CAS Registry Number.

1097201-63-2Upstream product

99-33-2 3,5-dinitrobenoyl chloride

1097201-63-2Downstream Products

1097201-63-2Relevant academic research and scientific papers

Stereoselective synthesis of novel aristeromycin analogues as potential antiviral agents

Bremond, Paul,Audran, Gerard,Monti, Honore,De Clercq, Erik

, p. 3253 - 3260 (2008)

A series of 3′-methyl-branched and purine-modified analogues of aristeromycin were synthesized via the SN2 displacement of a key triflate, which was prepared from a readily available enantiopure building block in eight steps. The synthesized compounds were evaluated as potential antiviral agents against important viruses. Only the 2,6-diaminopurine derivative exhibited moderate activity against vesicular stomatitis virus.

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