Cas 55008-35-0,2-[1-(2,4-Dimethoxy-phenyl)-meth-(Z)-ylidene]-4,8-dimethoxy-benzo[1,2-b;5,4-b']difuran-3-one

55008-35-0

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Basic information

Product Name: 2-[1-(2,4-Dimethoxy-phenyl)-meth-(Z)-ylidene]-4,8-dimethoxy-benzo[1,2-b;5,4-b']difuran-3-one
Synonyms: 2-[1-(2,4-Dimethoxy-phenyl)-meth-(Z)-ylidene]-4,8-dimethoxy-benzo[1,2-b;5,4-b']difuran-3-one
CAS NO:55008-35-0
Molecular Formula:
Molecular Weight: 382.37
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-[1-(2,4-Dimethoxy-phenyl)-meth-(Z)-ylidene]-4,8-dimethoxy-benzo[1,2-b;5,4-b']difuran-3-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-[1-(2,4-Dimethoxy-phenyl)-meth-(Z)-ylidene]-4,8-dimethoxy-benzo[1,2-b;5,4-b']difuran-3-one(55008-35-0)
EPA Substance Registry System: 2-[1-(2,4-Dimethoxy-phenyl)-meth-(Z)-ylidene]-4,8-dimethoxy-benzo[1,2-b;5,4-b']difuran-3-one(55008-35-0)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 55008-35-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 55008-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,0 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55008-35:
(7*5)+(6*5)+(5*0)+(4*0)+(3*8)+(2*3)+(1*5)=100
100 % 10 = 0
So 55008-35-0 is a valid CAS Registry Number.

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55008-35-0Relevant academic research and scientific papers

Photochemical reaction of phenanthrenequinone with some new aurones derived from khellin and visnagin

Nada,Zayed,El Din, N. Khir,El-Saidi,Hefny

, p. 1293 - 1302 (2002)

Phenanthrenequinone 2 and aurones 5a-h are potentially capable of undergoing an interesting photochemical reaction leading to the formation of the adducts 6a-h. The structures of the 1,4-dioxine derivatives 6a-h were firmly established on the basis of analytical data and spectroscopic evidences.

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