Cas 911798-58-8,2-(5,7-dimethoxy-2-(4-methoxyphenyl)spiro<chromane-4,2'-<1,3>dioxolan-8-yl>)-6-methoxy-2,3-dihydrobenzofuran-3-one

911798-58-8

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Basic information

Product Name: 2-(5,7-dimethoxy-2-(4-methoxyphenyl)spirodioxolan-8-yl>)-6-methoxy-2,3-dihydrobenzofuran-3-one
Synonyms: 2-(5,7-dimethoxy-2-(4-methoxyphenyl)spirodioxolan-8-yl>)-6-methoxy-2,3-dihydrobenzofuran-3-one
CAS NO:911798-58-8
Molecular Formula:
Molecular Weight: 520.536
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: 2-(5,7-dimethoxy-2-(4-methoxyphenyl)spirodioxolan-8-yl>)-6-methoxy-2,3-dihydrobenzofuran-3-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-(5,7-dimethoxy-2-(4-methoxyphenyl)spirodioxolan-8-yl>)-6-methoxy-2,3-dihydrobenzofuran-3-one(911798-58-8)
EPA Substance Registry System: 2-(5,7-dimethoxy-2-(4-methoxyphenyl)spirodioxolan-8-yl>)-6-methoxy-2,3-dihydrobenzofuran-3-one(911798-58-8)

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: 911798-58-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 911798-58-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,7,9 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 911798-58:
(8*9)+(7*1)+(6*1)+(5*7)+(4*9)+(3*8)+(2*5)+(1*8)=198
198 % 10 = 8
So 911798-58-8 is a valid CAS Registry Number.

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911798-58-8Relevant academic research and scientific papers

Aryllead Triacetates as Synthons for the Synthesis of Biflavonoids. Part 1. Synthesis and Reactivity of a Flavanonyllead Triacetate

Donnelly, Dervilla M. X.,Fitzpatrick, Brendan M.,Finet, Jean-Pierre

, p. 1791 - 1796 (2007/10/02)

The 8-triacetoxyplumbylflavane derivative 11 was prepared in 4 steps in 28percent overall yield from 4',5,7-flavanone.It reacted with the benzofuranone allyl β-keto ester 12 to yield a 8-(benzofuran-2-yl)flavanone 13 in 66percent.Removal of the allyl este

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