Cas 791610-18-9,7-(<i>tert</i>-butyl-diphenyl-silanyloxy)-2,2-dimethyl-3-oxo-heptanoic acid benzyl ester

791610-18-9

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Basic information

Product Name: 7-(tert-butyl-diphenyl-silanyloxy)-2,2-dimethyl-3-oxo-heptanoic acid benzyl ester
Synonyms: 7-(tert-butyl-diphenyl-silanyloxy)-2,2-dimethyl-3-oxo-heptanoic acid benzyl ester
CAS NO:791610-18-9
Molecular Formula:
Molecular Weight: 516.753
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: 7-(tert-butyl-diphenyl-silanyloxy)-2,2-dimethyl-3-oxo-heptanoic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 7-(tert-butyl-diphenyl-silanyloxy)-2,2-dimethyl-3-oxo-heptanoic acid benzyl ester(791610-18-9)
EPA Substance Registry System: 7-(tert-butyl-diphenyl-silanyloxy)-2,2-dimethyl-3-oxo-heptanoic acid benzyl ester(791610-18-9)

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: 791610-18-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 791610-18-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,1,6,1 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 791610-18:
(8*7)+(7*9)+(6*1)+(5*6)+(4*1)+(3*0)+(2*1)+(1*8)=169
169 % 10 = 9
So 791610-18-9 is a valid CAS Registry Number.

791610-18-9Upstream product

74-88-4 methyl iodide

791610-18-9Downstream Products

791610-19-0 8-(tert-butyl-diphenyl-silanyloxy)-1-diazo-3,3-dimethyl-octane-2,4-dione

791610-18-9Relevant academic research and scientific papers

Synthesis of cyclic hemiketals and spiroketals from dioxanorbornanes

Winkler, Jeffrey D.,Mikochik, Peter J.

, p. 3735 - 3737 (2004)

(Chemical Equation Presented) A new method for the synthesis of substituted pyranone hemiketals from dioxanorbornanes via Sml2 is described. Also reported is a synthesis of spiro[4.5]ketals from analogous intermediates via acid-promoted deprote

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