Cas 195200-24-9,Ethanone, 1-[2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-[(2,4-dinitrobenzoyl)oxy]-4- methyl-3-cyclohexen-1-yl]-

195200-24-9

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Basic information

Product Name: Ethanone, 1-[2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-[(2,4-dinitrobenzoyl)oxy]-4- methyl-3-cyclohexen-1-yl]-
Synonyms:
CAS NO:195200-24-9
Molecular Formula: C22H30N2O8Si
Molecular Weight: 478.574
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: Ethanone, 1-[2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-[(2,4-dinitrobenzoyl)oxy]-4- methyl-3-cyclohexen-1-yl]-(CAS DataBase Reference)
NIST Chemistry Reference: Ethanone, 1-[2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-[(2,4-dinitrobenzoyl)oxy]-4- methyl-3-cyclohexen-1-yl]-(195200-24-9)
EPA Substance Registry System: Ethanone, 1-[2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-[(2,4-dinitrobenzoyl)oxy]-4- methyl-3-cyclohexen-1-yl]-(195200-24-9)

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: 195200-24-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 195200-24-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,2,0 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 195200-24:
(8*1)+(7*9)+(6*5)+(5*2)+(4*0)+(3*0)+(2*2)+(1*4)=119
119 % 10 = 9
So 195200-24-9 is a valid CAS Registry Number.

195200-24-9Upstream product

195200-24-9Downstream Products

195200-24-9Relevant academic research and scientific papers

α-Acetyl- and α-Cyanovinyl 2,4-Dinitrophenyl Carboxylate as Useful Ketene Equivalents for the Diels-Alder Reaction

MaGee, David I.,Lee, May Ling

, p. 786 - 788 (1997)

Two ketene equivalents (5 and 35) have been developed for use in the Diels-Alder reaction. These dienophiles exhibit a marked increase in reactivity in comparison with the more conventional acetoxyacrylonitrile. Conversions of the cycloadducts to the requisite ketones occurs under mild, and moderate to high yielding conditions.

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