Cas 796-09-8,(E)-3-(amino(phenyl)methylene)-6-phenyl-2H-pyran-2,4(3H)-dione

796-09-8

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Basic information

Product Name: (E)-3-(amino(phenyl)methylene)-6-phenyl-2H-pyran-2,4(3H)-dione
Synonyms: (E)-3-(amino(phenyl)methylene)-6-phenyl-2H-pyran-2,4(3H)-dione
CAS NO:796-09-8
Molecular Formula:
Molecular Weight: 291.306
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: (E)-3-(amino(phenyl)methylene)-6-phenyl-2H-pyran-2,4(3H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: (E)-3-(amino(phenyl)methylene)-6-phenyl-2H-pyran-2,4(3H)-dione(796-09-8)
EPA Substance Registry System: (E)-3-(amino(phenyl)methylene)-6-phenyl-2H-pyran-2,4(3H)-dione(796-09-8)

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: 796-09-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 796-09-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,9 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 796-09:
(5*7)+(4*9)+(3*6)+(2*0)+(1*9)=98
98 % 10 = 8
So 796-09-8 is a valid CAS Registry Number.

796-09-8Upstream product

57689-80-2 (E)-3-(hydroxy(phenyl)methylene)-6-phenyl-2H-pyran-2,4(3H)-dione

796-09-8Downstream Products

796-09-8Relevant academic research and scientific papers

A novel synthetic approach to pyran-2,4-dione scaffold production: Microwave-assisted dimerization, cyclization, and expeditious regioselective conversion into β-enamino-pyran-2,4-diones

Sarhan, Ahmed A.M.,Haukka, Matti,Barakat, Assem,Boraei, Ahmed T.A.

supporting information, (2020/12/07)

Here, we report a novel, green, simple, low-cost, and rapid methodology for the high-yield production of pyran-2,4-dione scaffolds under microwave irradiation. Regio- and stereoselective conversions of β-diketone systems into β-enaminones were achieved us

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