Cas 1300749-63-6,tetraethyl 5,8-dimethyl-6-((trimethylsilyl)oxy)naphthalene-2,2,3,3(1H,4H)-tetracarboxylate

1300749-63-6

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Basic information

Product Name: tetraethyl 5,8-dimethyl-6-((trimethylsilyl)oxy)naphthalene-2,2,3,3(1H,4H)-tetracarboxylate
Synonyms: tetraethyl 5,8-dimethyl-6-((trimethylsilyl)oxy)naphthalene-2,2,3,3(1H,4H)-tetracarboxylate
CAS NO:1300749-63-6
Molecular Formula:
Molecular Weight: 536.695
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 5,8-dimethyl-6-((trimethylsilyl)oxy)naphthalene-2,2,3,3(1H,4H)-tetracarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tetraethyl 5,8-dimethyl-6-((trimethylsilyl)oxy)naphthalene-2,2,3,3(1H,4H)-tetracarboxylate(1300749-63-6)
EPA Substance Registry System: tetraethyl 5,8-dimethyl-6-((trimethylsilyl)oxy)naphthalene-2,2,3,3(1H,4H)-tetracarboxylate(1300749-63-6)

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: 1300749-63-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1300749-63-6 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 1300749-63:
(9*1)+(8*3)+(7*0)+(6*0)+(5*7)+(4*4)+(3*9)+(2*6)+(1*3)=126
126 % 10 = 6
So 1300749-63-6 is a valid CAS Registry Number.

1300749-63-6Upstream product

4071-85-6 trimetylsilylketene

1300749-63-6Downstream Products

1300749-63-6Relevant 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

, p. 7719 - 7721 (2011)

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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