Cas 1300749-60-3,tetraethyl 6-ethyl-6-(4-fluorophenyl)-5,8-dimethyl-7-oxo-6,7-dihydronaphthalene-2,2,3,3(1H,4H)-tetracarboxylate

1300749-60-3

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Basic information

Product Name: tetraethyl 6-ethyl-6-(4-fluorophenyl)-5,8-dimethyl-7-oxo-6,7-dihydronaphthalene-2,2,3,3(1H,4H)-tetracarboxylate
Synonyms: tetraethyl 6-ethyl-6-(4-fluorophenyl)-5,8-dimethyl-7-oxo-6,7-dihydronaphthalene-2,2,3,3(1H,4H)-tetracarboxylate
CAS NO:1300749-60-3
Molecular Formula:
Molecular Weight: 586.655
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: tetraethyl 6-ethyl-6-(4-fluorophenyl)-5,8-dimethyl-7-oxo-6,7-dihydronaphthalene-2,2,3,3(1H,4H)-tetracarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tetraethyl 6-ethyl-6-(4-fluorophenyl)-5,8-dimethyl-7-oxo-6,7-dihydronaphthalene-2,2,3,3(1H,4H)-tetracarboxylate(1300749-60-3)
EPA Substance Registry System: tetraethyl 6-ethyl-6-(4-fluorophenyl)-5,8-dimethyl-7-oxo-6,7-dihydronaphthalene-2,2,3,3(1H,4H)-tetracarboxylate(1300749-60-3)

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: 1300749-60-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1300749-60-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,0,7,4 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1300749-60:
(9*1)+(8*3)+(7*0)+(6*0)+(5*7)+(4*4)+(3*9)+(2*6)+(1*0)=123
123 % 10 = 3
So 1300749-60-3 is a valid CAS Registry Number.

1300749-60-3Upstream product

1185154-78-2 2-(4-fluorophenyl)but-1-en-1-one

1300749-60-3Downstream Products

1300749-60-3Relevant academic research and scientific papers

Ni-catalyzed ketene cycloaddition: A system that resists the formation of decarbonylation side products

Kumar, Puneet,Troast, Dawn M.,Cella, Rodrigo,Louie, Janis

supporting information; experimental part, p. 7719 - 7721 (2011/08/03)

Ni-phosphine complexes were used as catalysts for the cycloaddition of various ketenes and diynes. In general, 2,4-cyclohexadienones were formed instead of products arising from decarbonylation of the ketenes.

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