Cas 90606-69-2,1H-Naphth[2,3-f]isoindole-1,3(2H)-dione, 3a,4,11,11a-tetrahydro-5,6,8-trimethoxy-2-phenyl-4-[2-(trimethylsilyl)eth oxy]-

90606-69-2

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Basic information

Product Name: 1H-Naphth[2,3-f]isoindole-1,3(2H)-dione, 3a,4,11,11a-tetrahydro-5,6,8-trimethoxy-2-phenyl-4-[2-(trimethylsilyl)eth oxy]-
Synonyms:
CAS NO:90606-69-2
Molecular Formula: C30H35NO6Si
Molecular Weight: 533.697
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: 1H-Naphth[2,3-f]isoindole-1,3(2H)-dione, 3a,4,11,11a-tetrahydro-5,6,8-trimethoxy-2-phenyl-4-[2-(trimethylsilyl)eth oxy]-(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Naphth[2,3-f]isoindole-1,3(2H)-dione, 3a,4,11,11a-tetrahydro-5,6,8-trimethoxy-2-phenyl-4-[2-(trimethylsilyl)eth oxy]-(90606-69-2)
EPA Substance Registry System: 1H-Naphth[2,3-f]isoindole-1,3(2H)-dione, 3a,4,11,11a-tetrahydro-5,6,8-trimethoxy-2-phenyl-4-[2-(trimethylsilyl)eth oxy]-(90606-69-2)

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: 90606-69-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 90606-69-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,0 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90606-69:
(7*9)+(6*0)+(5*6)+(4*0)+(3*6)+(2*6)+(1*9)=132
132 % 10 = 2
So 90606-69-2 is a valid CAS Registry Number.

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90606-69-2Relevant academic research and scientific papers

Aureolic Acid Antibiotics: Synthesis of Naphthocyclobutene Precursors

Datta, Subhash C.,Franck, Richard W.,Noire, Paul D.

, p. 2785 - 2791 (2007/10/02)

The use of the dianion of 1,2-dicarbomethoxycyclobutane, a method introduced by Garrett, has been exploited to produce naphthocyclobutenes with methoxy groups in the naphtho moiety.A highly regioselective functionalization of the cyclobutene ring has been

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