Cas 1366465-26-0,4-tert-butyl 1-((1S,2R)-2-phenylcyclohexyl) 2-((tert-butyldimethylsilyl)oxy)-2-((E)-1,5-di(furan-2-yl)-3-oxopent-4-en-1-yl)succinate

1366465-26-0

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Basic information

Product Name: 4-tert-butyl 1-((1S,2R)-2-phenylcyclohexyl) 2-((tert-butyldimethylsilyl)oxy)-2-((E)-1,5-di(furan-2-yl)-3-oxopent-4-en-1-yl)succinate
Synonyms: 4-tert-butyl 1-((1S,2R)-2-phenylcyclohexyl) 2-((tert-butyldimethylsilyl)oxy)-2-((E)-1,5-di(furan-2-yl)-3-oxopent-4-en-1-yl)succinate
CAS NO:1366465-26-0
Molecular Formula:
Molecular Weight: 676.923
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: 4-tert-butyl 1-((1S,2R)-2-phenylcyclohexyl) 2-((tert-butyldimethylsilyl)oxy)-2-((E)-1,5-di(furan-2-yl)-3-oxopent-4-en-1-yl)succinate(CAS DataBase Reference)
NIST Chemistry Reference: 4-tert-butyl 1-((1S,2R)-2-phenylcyclohexyl) 2-((tert-butyldimethylsilyl)oxy)-2-((E)-1,5-di(furan-2-yl)-3-oxopent-4-en-1-yl)succinate(1366465-26-0)
EPA Substance Registry System: 4-tert-butyl 1-((1S,2R)-2-phenylcyclohexyl) 2-((tert-butyldimethylsilyl)oxy)-2-((E)-1,5-di(furan-2-yl)-3-oxopent-4-en-1-yl)succinate(1366465-26-0)

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: 1366465-26-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1366465-26-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,6,4,6 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1366465-26:
(9*1)+(8*3)+(7*6)+(6*6)+(5*4)+(4*6)+(3*5)+(2*2)+(1*6)=180
180 % 10 = 0
So 1366465-26-0 is a valid CAS Registry Number.

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1366465-26-0Relevant academic research and scientific papers

Three-component glycolate michael reactions of enolates, silyl glyoxylates, and α,β-enones

Schmitt, Daniel C.,Malow, Ericka J.,Johnson, Jeffrey S.

, p. 3246 - 3251 (2012)

Silyl glyoxylates react with enolates and enones to afford either glycolate aldol or Michael adducts. Product identity is controlled by the countercation associated with the enolate. Reformatsky nucleophiles in the presence of additional Zn(OTf)2/su

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