Cas 140860-92-0,Quinoline, 1,2,3,5,6,7,8,8a-octahydro-2-(4-methoxyphenyl)-1-phenyl-4-[(trimethylsil yl)oxy]-, trans-

140860-92-0

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Basic information

Product Name: Quinoline, 1,2,3,5,6,7,8,8a-octahydro-2-(4-methoxyphenyl)-1-phenyl-4-[(trimethylsil yl)oxy]-, trans-
Synonyms:
CAS NO:140860-92-0
Molecular Formula: C25H33NO2Si
Molecular Weight: 407.628
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: Quinoline, 1,2,3,5,6,7,8,8a-octahydro-2-(4-methoxyphenyl)-1-phenyl-4-[(trimethylsil yl)oxy]-, trans-(CAS DataBase Reference)
NIST Chemistry Reference: Quinoline, 1,2,3,5,6,7,8,8a-octahydro-2-(4-methoxyphenyl)-1-phenyl-4-[(trimethylsil yl)oxy]-, trans-(140860-92-0)
EPA Substance Registry System: Quinoline, 1,2,3,5,6,7,8,8a-octahydro-2-(4-methoxyphenyl)-1-phenyl-4-[(trimethylsil yl)oxy]-, trans-(140860-92-0)

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: 140860-92-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 140860-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,8,6 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 140860-92:
(8*1)+(7*4)+(6*0)+(5*8)+(4*6)+(3*0)+(2*9)+(1*2)=120
120 % 10 = 0
So 140860-92-0 is a valid CAS Registry Number.

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140860-92-0Relevant academic research and scientific papers

High degree of exo selectivity in imino Diels-Alder reactions catalyzed by tert-butyldimethylsilyltriflate

Nogue,Paugam,Wartski

, p. 1265 - 1268 (2007/10/02)

Diels-Alder reactions of silyloxydiene 1 derived from 1-acetylcyclohexene with imines 2b and 2c occur with high exo selectivity depending upon experimental conditions: exo cycloadducts 3b-c are exclusively formed under kinetic control using tert-butyldime

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