Cas 874913-13-0,1,4,8,10-Undecatetraen-3-one, 9-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1,11-diphenyl-4-(triethylsilyl)-, (1E,4E,8Z,10E)-

874913-13-0

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Basic information

Product Name: 1,4,8,10-Undecatetraen-3-one, 9-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1,11-diphenyl-4-(triethylsilyl)-, (1E,4E,8Z,10E)-
Synonyms:
CAS NO:874913-13-0
Molecular Formula: C35H50O2Si2
Molecular Weight: 558.952
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: 1,4,8,10-Undecatetraen-3-one, 9-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1,11-diphenyl-4-(triethylsilyl)-, (1E,4E,8Z,10E)-(CAS DataBase Reference)
NIST Chemistry Reference: 1,4,8,10-Undecatetraen-3-one, 9-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1,11-diphenyl-4-(triethylsilyl)-, (1E,4E,8Z,10E)-(874913-13-0)
EPA Substance Registry System: 1,4,8,10-Undecatetraen-3-one, 9-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1,11-diphenyl-4-(triethylsilyl)-, (1E,4E,8Z,10E)-(874913-13-0)

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: 874913-13-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 874913-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,9,1 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 874913-13:
(8*8)+(7*7)+(6*4)+(5*9)+(4*1)+(3*3)+(2*1)+(1*3)=200
200 % 10 = 0
So 874913-13-0 is a valid CAS Registry Number.

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874913-13-0Relevant academic research and scientific papers

Complexation-initiated intramolecular [4+2] cycloaddition: Construction of bridged-type cycloadducts

Iwasawa, Nobuharu,Inaba, Kennichi,Nakayama, Satoko,Aoki, Masao

, p. 7447 - 7450 (2005)

(Chemical Equation Presented) The characteristic structural features of [(alkyne)Co2(CO)6] complexes were used to achieve bridged-type intramolecular [4 + 2] cycloaddition reactions. The reaction of such complexes bearing a siloxydie

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