Cas 98568-78-6,4H-1-Benzopyran-4-one, 8-[2,3-dimethoxy-5-(7-methoxy-4-oxo-4H-1-benzopyran-2-yl)phenyl]-7- methoxy-2-(3,4,5-trimethoxyphenyl)-

98568-78-6

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Basic information

Product Name: 4H-1-Benzopyran-4-one, 8-[2,3-dimethoxy-5-(7-methoxy-4-oxo-4H-1-benzopyran-2-yl)phenyl]-7- methoxy-2-(3,4,5-trimethoxyphenyl)-
Synonyms:
CAS NO:98568-78-6
Molecular Formula: C37H32O11
Molecular Weight: 652.654
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: 4H-1-Benzopyran-4-one, 8-[2,3-dimethoxy-5-(7-methoxy-4-oxo-4H-1-benzopyran-2-yl)phenyl]-7- methoxy-2-(3,4,5-trimethoxyphenyl)-(CAS DataBase Reference)
NIST Chemistry Reference: 4H-1-Benzopyran-4-one, 8-[2,3-dimethoxy-5-(7-methoxy-4-oxo-4H-1-benzopyran-2-yl)phenyl]-7- methoxy-2-(3,4,5-trimethoxyphenyl)-(98568-78-6)
EPA Substance Registry System: 4H-1-Benzopyran-4-one, 8-[2,3-dimethoxy-5-(7-methoxy-4-oxo-4H-1-benzopyran-2-yl)phenyl]-7- methoxy-2-(3,4,5-trimethoxyphenyl)-(98568-78-6)

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: 98568-78-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 98568-78-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,5,6 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 98568-78:
(7*9)+(6*8)+(5*5)+(4*6)+(3*8)+(2*7)+(1*8)=206
206 % 10 = 6
So 98568-78-6 is a valid CAS Registry Number.

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98568-78-6Relevant academic research and scientific papers

Naturally Occuring Biflavonoid Derivatives: Part VII - Galluflavanone, a New Biflavonoid from Semecarpus anacardium Linn.

Murthy, S. S. N.

, p. 398 - 402 (2007/10/02)

A new biflavonoid, named as galluflavanone and isolated from the alcoholic extract of the nut shells of Semecarpus anacardium Linn., has been dehydrogenated with iodine and potassium acetate in gl. acetic acid to the corresponding, relatively more stable biflavone designated as SA6.The structure of galluflavanone has been established on the basis of chemical and spectroscopic evidences.

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