Cas 1394170-59-2,1-(2-((tert-butyl((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)(4-methoxyphenyl)silyl)oxy)ethyl)-4'-methoxy-[1,1'-biphenyl]-4(1H)-one

1394170-59-2

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Basic information

Product Name: 1-(2-((tert-butyl((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)(4-methoxyphenyl)silyl)oxy)ethyl)-4'-methoxy-[1,1'-biphenyl]-4(1H)-one
Synonyms: 1-(2-((tert-butyl((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)(4-methoxyphenyl)silyl)oxy)ethyl)-4'-methoxy-[1,1'-biphenyl]-4(1H)-one
CAS NO:1394170-59-2
Molecular Formula:
Molecular Weight: 602.646
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-(2-((tert-butyl((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)(4-methoxyphenyl)silyl)oxy)ethyl)-4'-methoxy-[1,1'-biphenyl]-4(1H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-(2-((tert-butyl((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)(4-methoxyphenyl)silyl)oxy)ethyl)-4'-methoxy-[1,1'-biphenyl]-4(1H)-one(1394170-59-2)
EPA Substance Registry System: 1-(2-((tert-butyl((1,1,1,3,3,3-hexafluoropropan-2-yl)oxy)(4-methoxyphenyl)silyl)oxy)ethyl)-4'-methoxy-[1,1'-biphenyl]-4(1H)-one(1394170-59-2)

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: 1394170-59-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1394170-59-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,1,7 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1394170-59:
(9*1)+(8*3)+(7*9)+(6*4)+(5*1)+(4*7)+(3*0)+(2*5)+(1*9)=172
172 % 10 = 2
So 1394170-59-2 is a valid CAS Registry Number.

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1394170-59-2Relevant academic research and scientific papers

Oxidative ipso -Rearrangement performed by a hypervalent iodine reagent and its application

Jacquemot, Guillaume,Canesi, Sylvain

, p. 7588 - 7594 (2012/10/29)

An oxidative ipso-rearrangement mediated by a hypervalent iodine reagent that enables rapid generation of a functionalized dienone system containing a quaternary carbon center connected to several sp2 centers has been developed. The process occurs through transfer of an aryl group from a silyl segment present on the lateral chain. As an illustration of the potential of this transformation, a total synthesis of sceletenone, a small alkaloid, is described.

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