Cas 112476-46-7,2,4-Pentadienamide, N-[1-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2-propenyl]-N-(phenyl methyl)-, (E)-

112476-46-7

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Basic information

Product Name: 2,4-Pentadienamide, N-[1-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2-propenyl]-N-(phenyl methyl)-, (E)-
Synonyms:
CAS NO:112476-46-7
Molecular Formula: C32H37NO2Si
Molecular Weight: 495.737
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: 2,4-Pentadienamide, N-[1-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2-propenyl]-N-(phenyl methyl)-, (E)-(CAS DataBase Reference)
NIST Chemistry Reference: 2,4-Pentadienamide, N-[1-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2-propenyl]-N-(phenyl methyl)-, (E)-(112476-46-7)
EPA Substance Registry System: 2,4-Pentadienamide, N-[1-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2-propenyl]-N-(phenyl methyl)-, (E)-(112476-46-7)

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: 112476-46-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112476-46-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,4,7 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112476-46:
(8*1)+(7*1)+(6*2)+(5*4)+(4*7)+(3*6)+(2*4)+(1*6)=107
107 % 10 = 7
So 112476-46-7 is a valid CAS Registry Number.

112476-46-7Upstream product

112476-46-7Downstream Products

112476-42-3 2-Benzyl-3-(tert-butyl-diphenyl-silanyloxymethyl)-2,3,3a,4,5,7a-hexahydro-isoindol-1-one

112476-46-7Relevant academic research and scientific papers

STEREOSELECTIVITY IN INTRAMOLECULAR DIELS-ALDER REACTION II : INFLUENCE OF ALKYL SUBSTITUENT ON CYCLIZATION OF AZATRIENES

Guy, A.,Lemaire, M.,Graillot, Y.,Negre, M.,Guette, J. P.

, p. 2969 - 2972 (2007/10/02)

Substitution of the allylic moiety of azatrienes of functionalized alkyl groups permits high chemical yields and stereoselectivity during I.M.D.A cyclization.Substituted hydroisoindoles, precursors for natural and pharmaceutical products were prepared with good yields and selectivity.

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