Cas 852674-77-2,[1-(<i>tert</i>-butyl-diphenyl-silanyloxymethyl)-4,10-dioxo-undecyl]-carbamic acid <i>tert</i>-butyl ester

852674-77-2

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Basic information

Product Name: [1-(tert-butyl-diphenyl-silanyloxymethyl)-4,10-dioxo-undecyl]-carbamic acid tert-butyl ester
Synonyms: [1-(tert-butyl-diphenyl-silanyloxymethyl)-4,10-dioxo-undecyl]-carbamic acid tert-butyl ester
CAS NO:852674-77-2
Molecular Formula:
Molecular Weight: 567.841
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-(tert-butyl-diphenyl-silanyloxymethyl)-4,10-dioxo-undecyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [1-(tert-butyl-diphenyl-silanyloxymethyl)-4,10-dioxo-undecyl]-carbamic acid tert-butyl ester(852674-77-2)
EPA Substance Registry System: [1-(tert-butyl-diphenyl-silanyloxymethyl)-4,10-dioxo-undecyl]-carbamic acid tert-butyl ester(852674-77-2)

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: 852674-77-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 852674-77-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,2,6,7 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 852674-77:
(8*8)+(7*5)+(6*2)+(5*6)+(4*7)+(3*4)+(2*7)+(1*7)=202
202 % 10 = 2
So 852674-77-2 is a valid CAS Registry Number.

852674-77-2Upstream product

852674-77-2Downstream Products

852674-77-2Relevant academic research and scientific papers

An N-acyliminium cyclization approach to a total synthesis of (+)-cylindricine C

Liu, Jia,Swidorski, Jacob J.,Peters, Scott D.,Hsung, Richard P.

, p. 3898 - 3902 (2007/10/03)

Details of problems and solutions encountered during the development of an enantioselective total synthesis of (+)-cylindricine C are described here. The total synthesis itself was accomplished in 8 steps, featuring an N-acyliminium cyclization strategy,

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